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Electrolyte Drink

Test product 1 for Edema

N/A
Waitlist Available
Led By Jeremy Townsend, PhD
Research Sponsored by Liquid I.V.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Healthy males 18-35 years old at the time of screening. Participants need to be competent i.e., able to understand what is to take place and able to provide a free decision on agreeing to the activity/taking part in the study. Participants must be able to read and understand study instructions and any other relevant study documents. Willing to following the lifestyle and dietary restrictions as detailed in the Information Sheet for study.
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, average of 6 weeks
Awards & highlights

Study Summary

This trial will test the effects of two new hydration beverage formulas on rehydration in healthy adults. The formulas contain electrolytes and vitamins, and are designed to allow water to be absorbed into the bloodstream more quickly.

Eligible Conditions
  • Edema
  • Beverage Hydration Index
  • Dehydration

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, average of 6 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion, average of 6 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Beverage hydration index
Hydration status

Trial Design

3Treatment groups
Experimental Treatment
Placebo Group
Group I: Test Product 2Experimental Treatment1 Intervention
Participants will consume test product 2 during one experimental visit.
Group II: Test Product 1Experimental Treatment1 Intervention
Participants will consume test product 1 during one experimental visit.
Group III: PlaceboPlacebo Group1 Intervention
Participants will consume placebo during one experimental visit.

Find a Location

Who is running the clinical trial?

Lipscomb UniversityOTHER
4 Previous Clinical Trials
73 Total Patients Enrolled
Liquid I.V.Lead Sponsor
3 Previous Clinical Trials
72 Total Patients Enrolled
Jeremy Townsend, PhDPrincipal InvestigatorLipscomb University
1 Previous Clinical Trials
11 Total Patients Enrolled

Frequently Asked Questions

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

Who else is applying?

What state do they live in?
Ohio
What site did they apply to?
Lipscomb University
What portion of applicants met pre-screening criteria?
Did not meet criteria
~6 spots leftby Apr 2025