Calcium Gluconate

Osteomalacia, Hereditary disorder, Hypoparathyroidism + 16 more

Treatment

2 FDA approvals

20 Active Studies for Calcium Gluconate

What is Calcium Gluconate

Calcium gluconate

The Generic name of this drug

Treatment Summary

Calcium gluconate is a mineral supplement used to increase calcium in the diet. It is taken orally, but can also be injected into a vein to treat or prevent calcium deficiency-related conditions like osteoporosis or rickets. Each 10 mL of the injection contains 93 mg of elemental calcium, the equivalent of 1 gram of calcium gluconate. The solution has hydrochloric acid and/or sodium hydroxide added to it to adjust the pH balance.

Calcium Gluconate

is the brand name

Calcium Gluconate Overview & Background

Brand Name

Generic Name

First FDA Approval

How many FDA approvals?

Calcium Gluconate

Calcium gluconate

1990

13

Approved as Treatment by the FDA

Calcium gluconate, commonly known as Calcium Gluconate, is approved by the FDA for 2 uses such as Hypocalcemia and Hypocalcemia .

Hypocalcemia

Hypocalcemia

Effectiveness

How Calcium Gluconate Affects Patients

Calcium Gluconate is a form of calcium that is important for maintaining healthy nerve, muscle, and heart function. It is used to help keep the right amount of calcium in the body and prevent bone loss when taken as a pill. It may also reduce the risk of getting certain types of cancer.

How Calcium Gluconate works in the body

Calcium is important for many aspects of our bodies to work properly. It helps regulate the release and storage of hormones and neurotransmitters, helps absorb vitamin B12, and helps control blood clotting. Calcium is stored mostly in the bones, with smaller amounts in the blood. If we don't get enough calcium from our diet, our bodies will take it from the bones, which can lead to weakened bones. For this reason, it's important to get enough calcium in your diet to maintain healthy bones.

When to interrupt dosage

The prescribed dose of Calcium Gluconate is contingent upon the determined condition, like Postmenopausal Osteoporosis, Hypoparathyroidism and Bone and Bones. The dosage will differ, depending on the method of delivery (e.g. Powder - Oral or Capsule - Oral) displayed in the following table.

Condition

Dosage

Administration

Osteomalacia

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Osteoporosis, Postmenopausal

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Hereditary disorder

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Hypoparathyroidism

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Osteoporosis

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Hypophosphatemia

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Hypocalcemia

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

ergocalciferol

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Renal Tubular Disorder

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Lactating Women

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Hypocalcemia

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Liver Diseases

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Renal Insufficiency

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Vitamin D Deficiency

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Nutritional Rickets

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Rickets

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Otosclerosis

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Bone and Bones

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Bone and Bones

98.0 mg/mL, , 0.465 meq/mL, 94.0 mg/mL, 10.0 %, 650.0 mg, 648.0 mg, 600.0 mg, 155.0 mg, 538.0 mg, 0.025 mg/mg, 500.0 mg, 700.0 mg, 60.0 mg, 94.0 mg, 2.55 %, 20.0 mg/mL, 100.0 mg/mL, 6.0 mg/mL, 112.0 mg/mL, 20.6 mg/mL, 10.0 mg/mL, 35.0 mg, 1.25 mg/mL, 0.4 mg/mg, 100.0 mg

, Intravenous, Injection, solution, Injection, solution - Intravenous, Solution, Solution - Intravenous, Liquid, Liquid - Intravenous, Oral, Tablet, Tablet - Oral, Liquid - Oral, Intramuscular; Intravenous, Solution - Intramuscular; Intravenous, Gel, Topical, Gel - Topical, Capsule - Oral, Capsule, Vaginal, Douche, Douche - Vaginal, Powder, Powder - Oral

Warnings

There are 20 known major drug interactions with Calcium Gluconate.

Common Calcium Gluconate Drug Interactions

Drug Name

Risk Level

Description

Calcium acetate

Major

The risk or severity of adverse effects can be increased when Calcium gluconate is combined with Calcium acetate.

Dobutamine

Minor

The therapeutic efficacy of Dobutamine can be decreased when used in combination with Calcium gluconate.

3-Aza-2,3-Dihydrogeranyl Diphosphate

Moderate

Calcium gluconate can cause a decrease in the absorption of 3-Aza-2,3-Dihydrogeranyl Diphosphate resulting in a reduced serum concentration and potentially a decrease in efficacy.

Acebutolol

Moderate

The therapeutic efficacy of Acebutolol can be decreased when used in combination with Calcium gluconate.

Acetyldigitoxin

Moderate

Calcium gluconate may increase the arrhythmogenic and cardiotoxic activities of Acetyldigitoxin.

Calcium Gluconate Toxicity & Overdose Risk

The lowest toxic dose of the drug in infants when administered intramuscularly is 10gm/kg, which can cause changes in the meninges. The lowest toxic dose when administered intramuscularly is 143mg/kg and can cause dermatitis. In mice, the lethal dose when administered intravenously is 950mg/kg and the lowest toxic dose when given orally is 10gm/kg.

Calcium Gluconate Novel Uses: Which Conditions Have a Clinical Trial Featuring Calcium Gluconate?

86 active trials are being conducted to explore the efficacy of Calcium Gluconate in mitigating Bone and Bones Conditions, Genetic Disorders and Hypocalcemia.

Condition

Clinical Trials

Trial Phases

Liver Diseases

0 Actively Recruiting

Rickets

2 Actively Recruiting

Early Phase 1, Not Applicable

Otosclerosis

0 Actively Recruiting

Hypocalcemia

0 Actively Recruiting

Osteoporosis

27 Actively Recruiting

Not Applicable, Phase 4, Phase 1, Phase 3, Phase 2

Lactating Women

0 Actively Recruiting

Hypocalcemia

0 Actively Recruiting

Osteoporosis, Postmenopausal

0 Actively Recruiting

ergocalciferol

1 Actively Recruiting

Phase 4

Renal Insufficiency

0 Actively Recruiting

Hereditary disorder

2 Actively Recruiting

Not Applicable

Renal Tubular Disorder

0 Actively Recruiting

Hypophosphatemia

1 Actively Recruiting

Phase 2

Bone and Bones

0 Actively Recruiting

Vitamin D Deficiency

0 Actively Recruiting

Osteomalacia

0 Actively Recruiting

Bone and Bones

0 Actively Recruiting

Hypoparathyroidism

3 Actively Recruiting

Not Applicable, Phase 2, Phase 1

Nutritional Rickets

0 Actively Recruiting

Patient Q&A Section about calcium gluconate

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

When should calcium gluconate be administered?

"Calcium gluconate is used to correct calcium deficiencies that cause problems such as muscle spasms, low calcium levels due to a lack of parathyroid hormone, and low calcium levels due to pregnancy or rapid growth."

Answered by AI

What is calcium gluconate an antidote for?

"Calcium gluconate is used as a cardioprotective agent in high blood potassium. It is also the antidote for magnesium sulfate toxicity."

Answered by AI

What is the effect of calcium gluconate?

"The following are symptoms of a heart attack: swelling, rapid weight gain, light-headed feeling, slow or irregular heartbeats, high levels of calcium in your blood, nausea, vomiting, constipation, increased thirst or urination, muscle weakness, bone pain, confusion, lack of energy, or feeling tired."

Answered by AI

How does calcium gluconate affect the heart?

"If calcium gluconate is injected too quickly, it can cause blood pressure to drop, the heart to beat slowly, and irregular heartbeats. In severe cases, a person may faint or their heart may stop altogether."

Answered by AI

Clinical Trials for Calcium Gluconate

Image of UC San Diego in San Diego, United States.

Epione Device for Bone Conditions

18+
All Sexes
San Diego, CA

The goal of this investigational device exemption is to evaluate the Epione assistance for introducer placement during percutaneous procedures in musculo-skeletic (MSK) structures of the pelvis and the spine in adults. The main question is the determination of the rate of feasible procedures assisted by the Epione device Participants will undergo their procedure(s) as planned by their physician. If they accept to participate to the study, the differences with standard of care will be: * The use of the Epione device to place the introducer(s), instead of freehand placement if they do not participate * Additional CT or CBCT scans during the procedure.

Waitlist Available
Has No Placebo

UC San Diego (+2 Sites)

Sean Tutton, MD

Quantum Surgical

Image of University of Waterloo in Waterloo, Canada.

Virtual Chiropractic Intervention for Spinal Fracture

18+
All Sexes
Waterloo, Canada

This study will determine feasibility of a chiropractor delivered virtual intervention for individuals following osteoporotic vertebral fracture. This pilot trial will have two parallel groups with a 1:1 ratio. Participants will be randomized to: 1) immediate receipt; or 2) waitlist usual care control and delayed receipt of VIVA 10 weeks post-randomization. VIVA is an intervention for people with vertebral fractures that covers four areas: pain management, safe movement, exercise, and nutrition. It includes print and video resources, and a framework for goal setting, selecting exercises, and teaching body mechanics. A chiropractor (DC) completes a virtual assessment and then leads twelve 1:1 virtual sessions (via Zoom) over eight weeks. Sessions start with brief education on a topic (e.g., safe movement, pain management, exercise, nutrition), followed by training and modeling of exercise and safe movement strategies, then goal setting, and action planning. This trial will be considered feasible if a) we recruit 14 people in eight months; b) 80% of participants complete the trial; and c) exercise adherence is 75%.

Recruiting
Has No Placebo

University of Waterloo

Have you considered Calcium Gluconate clinical trials?

We made a collection of clinical trials featuring Calcium Gluconate, we think they might fit your search criteria.
Go to Trials
Image of University of Maryland, Baltimore, Department of Epidemiology and Public Health, Division of Gerontology in Baltimore, United States.

OPTIONS Program for Osteoporosis

65+
All Sexes
Baltimore, MD

Osteoporosis is a disease that weakens bones so the bones may break easily. The risk for osteoporosis increases with age in both women and men. Osteoporosis affects 10 million older adults in the US. Osteoporosis is a common cause of broken bones in the hips and legs. Broken bones can lead to disability, nursing home placement, and death. Because of the dire consequences, a broken hip or leg is one of the most dreaded injuries for older adults. Many studies confirm that a simple regimen of exercise, healthy diet and bone-strengthening medications can improve overall recovery after a broken hip or leg. This regimen can prevent a person from becoming disabled, having future fractures, and even prevent death. Many older adults have surgery in a hospital after breaking a hip or leg. Then older adults go to a skilled nursing facility (SNF) for rehabilitation. Care in SNFs varies greatly. Some patients do not receive the regimen that the investigators know is most beneficial to improve bone health and recovery. Even patients who get exercise, healthy diet, and bone-strengthening medication in the SNF, may not continue with the regimen once patients go home. Therefore, the investigators want to implement and test OsteoPorotic fracTure preventION System (OPTIONS). OPTIONS is a program that will integrate the regimen into the care that is provided in SNFs and after discharge to the community. OPTONS will provide information about exercise, diet, and bone-strengthening medication. OPTIONS will provide doctors, clinical staff, patients, and care partners with the information these stakeholders need to carry out the best-practice regimen. The investigators are partnering with PointClickCare, a large cloud-based healthcare software provider, with SNFs and community care sites across the US. The investigators will include 32 SNFs from different US areas. The investigators will flip a coin to assign SNFs to the intervention (OPTIONS) or the control arm (enhanced usual care) of the study. Enhanced usual care is the care that is typically provided in SNFs after a fracture and adding information about a publicly available fall prevention toolkit. The investigators are using an "implementation science" approach that requires the investigators to get input from the OPTIONS study's vast stakeholder community throughout the study. The OPTIONS study's stakeholders include patients, care partners, clinicians, and professional organizations. The research question is, can using OPTIONS in SNFs and in the community after discharge improve physical function and quality of life in older people in the year after a hip or leg fracture? The investigators are measuring patient-reported outcomes. The investigators will include 1553 patients across the 32 facilities. The investigators have selected outcomes that are important to patients. Specifically, the investigators are measuring patient-reported function and quality of life. The investigators are also measuring patient-reported falls and fractures. The investigators will track the number of patients who die during the study. This study's hypothesis is that patients who receive OPTIONS will report better physical function (i.e., can walk and take better care of themselves) than those who receive enhanced usual care. The investigators also hypothesize that patients that receive OPTIONS will report a better quality of life than those who receive enhanced usual care. This study will provide sound data about the effectiveness of OPTIONS. OPTIONS could then be spread to other SNFs and community-based programs. This would ensure that all older people receive the right care after a hip or leg fracture.

Recruiting
Has No Placebo

University of Maryland, Baltimore, Department of Epidemiology and Public Health, Division of Gerontology (+1 Sites)

Denise Orwig, PhD

Image of Arthritis Research Canada in Vancouver, Canada.

Virtual Rehabilitation for Spinal Fracture

18+
All Sexes
Vancouver, Canada

Spine fractures are the most common fracture due to osteoporosis. They happen during falls or activities of daily life, like bending to tie shoes. Fractures of the spine can result in pain, which can sometimes last for a long time. Spine fractures can affect breathing, appetite, digestion, and mobility, and can restrict or modify people's work or daily activities. There are no standard rehabilitation programs after spine fracture, and patients often have to pay for rehabilitation. Rehabilitation can be hard to access, especially in rural or remote locations. It can be hard to find health care or rehabilitation providers who specialize in treating spine fractures. After reviewing research and consulting patients and health care providers to understand their experiences with spine fracture rehabilitation, the research team developed a toolkit for a virtual rehabilitation program for people with spine fractures, called VIVA. The research team wants to submit a grant for a clinical trial to implement VIVA in five provinces and determine if VIVA reduces pain and improves physical functioning and quality of life, and if the benefits outweigh the costs. Before this, the team proposes to do a pilot study to test how feasible it is to do a study of VIVA in three provinces.

Waitlist Available
Has No Placebo

Arthritis Research Canada (+5 Sites)

Lora Giangregorio, PhD

Have you considered Calcium Gluconate clinical trials?

We made a collection of clinical trials featuring Calcium Gluconate, we think they might fit your search criteria.
Go to Trials
Image of Marcus Institute for Aging Research, Hebrew SeniorLife in Boston, United States.

Injury Prevention Care Models for Osteoporosis

65+
All Sexes
Boston, MA

The goal of this clinical trial is to compare three care models for optimizing medications and preventing falls with broken bones in patients receiving rehabilitation after a hospitalization for a broken bone. The primary outcome is injurious falls, with secondary outcomes measuring how the process of care is changed and capturing patient-reported outcomes valued by stakeholders. The main questions this study aims to answer are: * Which of the three models is more effective in preventing falls with fractures? * What are the differences in patient-centered outcomes amongst the three models? These include pain, depression, anxiety, sleep, medication side effect burden, and fear of falling. * What are the differences in osteoporosis treatment and medication burden? The three care models are: a Deprescribing Care Model designed to reduce or stop fall-related medications, a Bone Heath Service Model designed to provide osteoporosis evaluation and management, and an Injury Prevention Service Model offering both services. 42 SNFs will participate in this study. The three models will be incorporated into the routine care of patients at these facilities who are receiving rehabilitation after a hospitalization for a fracture. All care models will be delivered remotely to patients in the SNF and after they transition home by a post-fracture nurse consultant supported by an interprofessional team. This study has three aims. See Detailed Description for more details. This ClinicalTrials.gov record represents the Comparative Effectiveness Aim of the protocol.

Waitlist Available
Has No Placebo

Marcus Institute for Aging Research, Hebrew SeniorLife (+1 Sites)

Cathleen S Colon-Emeric, MD, MHS

Image of University of Saskatchewan in Saskatoon, Canada.

Milk + Yogurt for Bone Health

19 - 30
All Sexes
Saskatoon, Canada

Milk and dairy products contain significant amounts of nutrients that contribute to optimal health - nutrients like calcium, vitamin D, and high-quality protein. Fermented milk products or fermented dairy products are dairy foods that have been fermented with certain bacteria. Yogurt is a fermented dairy product containing millions of beneficial bacteria. In this study, the invesgitagtors will look at the effect of milk (a non-fermented dairy product) and yogurt (a fermented dairy product) supplementation on bone health and the amount of fat and muscle mass in Canadian young adults over a 24-month period. While dairy products contain significant amounts of nutrients, the scientific community does not know the impact of long-term supplementation of fermented (i.e., yogurt) or non-fermented (i.e., milk) dairy food on bone health and the amount of fat and muscle mass in young adults. To fill this knowledge gap, the investigators will recruit participants with low calcium intake and assign them to three different groups: 1) milk (intervention) group; 2) yogurt (intervention) group; and 3) control group. The investigators will ask the participants in the milk group to drink 1.5 servings (375 mL) of milk per day for 24 months. Participants in the yogurt group will consume 2 servings (350 g) of yogurt per day for 24 months. Those in the control group will continue their usual diets. Using a randomized controlled trial design, the investigators will measure bone health parameters, hormonal indices related to bone metabolism, body composition (e.g., muscle mass, fat mass), and the number and composition of bacteria living in the gastrointestinal (GI) tract. The hypothesis is that supplementation with yogurt will have more positive effects on bone health indices, particularly femoral neck BMD as the primary outcome, than milk in Canadian adults aged 19-30 years. The secondary hypothesis is that supplementation with yogurt, as a fermented milk product, will have a more beneficial effect than milk on body composition measures. The data will provide valuable information for developing targeted health initiatives and marketing strategies regarding the benefits of fermented and non-fermented dairy product consumption.

Recruiting
Has No Placebo

University of Saskatchewan

Hassan Vatanparast, MD, PhD

Image of University of Kentucky in Lexington, United States.

Teriparatide vs Alendronate for Osteoporosis

18+
Female
Lexington, KY

Osteoporosis is a health problem of major proportions. It affects more than 40 million Americans and results in more than 2 million fractures annually among Medicare patients alone. Hospital admissions for osteoporotic fractures exceed those of heart attacks, strokes and breast cancer combined. Osteoporosis is commonly considered a disease associated with menopause. This estrogen deficiency related bone loss is characterized by high bone turnover with increased resorption without commensurate changes in bone formation. It is in contrast to age-related bone loss, which starts as early as in the fourth decade of life and continues with increasing age. Age-related bone loss is usually associated with lower bone turnover and decreased bone formation is the main abnormality. Current therapies do not address age-related bone loss and the special needs of the age-related osteoporosis population is currently ignored. This is to a great degree due to difficulties associated with the bone biopsy necessary for unequivocal determination of bone turnover status. Thus, the current standard of care relies on starting with an antiresorber, which is of limited effectiveness in age-related osteoporosis, and in fact impedes the effectiveness of the appropriate anabolic medication. In a current ongoing study - Novel precision medicine approach to treatment of osteoporosis based on bone turnover. EIRB#70781; efforts are focused on addressing this particular problem. Our follow-up study seeks to achieve one specific aim: to compare effectiveness of Alendronate vs Teriparatide after participants have been switched at the end of treatment at year one, to the other drug at year two for the same duration of treatment.

Phase 4
Waitlist Available

University of Kentucky

Paul Netzel, DNP

Have you considered Calcium Gluconate clinical trials?

We made a collection of clinical trials featuring Calcium Gluconate, we think they might fit your search criteria.
Go to Trials