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Brewed kombucha tea for Diabetes Mellitus
N/A
Waitlist Available
Led By Julie M Kapp, MPH, PhD
Research Sponsored by University of Missouri-Columbia
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline
Awards & highlights
Study Summary
This trial will study how kombucha affects glucose metabolism in humans.
Eligible Conditions
- Diabetes Mellitus
- High Blood Sugar
- Diabetes
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Blood glucose level
Fasting blood glucose level
Fasting insulin level.
+1 moreSecondary outcome measures
Blood pressure
Trial Design
4Treatment groups
Experimental Treatment
Active Control
Placebo Group
Group I: Intervention group 2: brewed kombuchaExperimental Treatment1 Intervention
8oz
Group II: Intervention group 1: commercial kombuchaExperimental Treatment1 Intervention
8oz
Group III: Control group 1: teaActive Control1 Intervention
8oz
Group IV: Control group 2: waterPlacebo Group1 Intervention
8oz
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Commercial kombucha tea
2019
N/A
~40
Brewed kombucha tea
2019
N/A
~40
Find a Location
Who is running the clinical trial?
University of Missouri-ColumbiaLead Sponsor
361 Previous Clinical Trials
627,961 Total Patients Enrolled
12 Trials studying Diabetes Mellitus
551,470 Patients Enrolled for Diabetes Mellitus
Julie M Kapp, MPH, PhDPrincipal InvestigatorUniversity of Missouri-Columbia
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You currently use any type of product that contains nicotine.You have been diagnosed with COPD (a chronic lung disease).You have a long-term problem with drinking too much alcohol.You have been diagnosed with peripheral vascular disease.Participants must be between the ages of 30 and 65, regardless of gender.You are able to travel to the study location.You have an autoimmune disease.You are pregnant or currently breastfeeding.You are considered overweight or obese based on your body mass index (BMI) being 25 or higher.You must be able to speak and understand English.You have been diagnosed with cancer.You have taken prebiotic or probiotic supplements in the last 3 months on a regular basis.
Research Study Groups:
This trial has the following groups:- Group 1: Intervention group 1: commercial kombucha
- Group 2: Control group 1: tea
- Group 3: Intervention group 2: brewed kombucha
- Group 4: Control group 2: water
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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