Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
ID06854471

Effects of Beverage Volume, Glycerol Concentration, and Sodium Concentration on Fluid Balance in Healthy Euhydrated Men and Women at Rest

Led by PepsiCo Global R&D · Updated on 2025-07-17

80

Participants Needed

3

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how different levels of sodium and glycerol in beverages, along with varying drink volumes, affect fluid balance in healthy adults who are well hydrated. The study aims to understand how these ingredients help the body keep fluids by reducing urine loss, which is important for maintaining overall body hydration. This research involves healthy men and women aged 18 to 50, who are generally physically active. Participants will consume different types of beverages that vary in electrolyte and glycerol content and volume, including a placebo beverage without electrolytes or glycerol. Each beverage is taken in three doses over 35 minutes, followed by a 25-minute rest period before measurements begin. The study includes multiple experimental beverage groups to compare how these factors influence fluid retention. During the study, participants will undergo repeated assessments over 210 minutes after drinking, including measurements of fluid balance, urine volume and concentration, blood markers like electrolytes and glucose, heart rate, and blood pressure. Participants will also report any gastrointestinal discomfort or headaches. Safety is monitored throughout the study, and menstrual cycle information is collected at screening. The trial runs until December 2025 and involves detailed monitoring of how beverages affect body hydration over time.

CONDITIONS

Brief Title

Effects of Beverage Volume, Glycerol Concentration, and Sodium Concentration on Fluid Balance in Healthy Euhydrated Men and Women at Rest

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female
  • Female participants must not be pregnant
  • Age between 18 and 50 years, inclusive
  • Recreationally active with light to moderate exercise at least 3 days per week for 30 minutes each
  • Non-smoker or quit smoking at least 6 months ago
  • Not taking medications that interfere with the study such as diuretics
  • No health conditions like cardiovascular, renal, or metabolic diseases that interfere with the study
  • Willing to avoid alcohol 24 hours before visits
  • Willing to fast overnight for about 8-12 hours
  • Willing to avoid vigorous exercise for 24 hours before visits
  • Willing to eat the same food the day before each visit
  • Provide written consent to participate
Not Eligible

You will not qualify if you...

  • Participated in any clinical trial within past 30 days
  • Participated in any PepsiCo trial within past 6 months
  • Has a condition or takes medication that may affect consent, study compliance, result interpretation, or safety
  • Employed by or closely related to someone employed by a company competing with Gatorade, unless disclosed and approved

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Intervention

Duration - Up to 6 separate beverage testing days

Participants consume different beverages with varying volumes and concentrations of glycerol and sodium, followed by rest and fluid balance assessments.

6 visits (in-person) for beverage testing

Trial Site Locations

Total: 3 locations

1

IMG Academy/GSSI Bradenton Gatorade Sports Science Institute

Bradenton, Florida, United States, 34210

Actively Recruiting

2

GCP Research

St. Petersburg, Florida, United States, 33705

Actively Recruiting

3

Gatorade Sports Science Institute

Valhalla, New York, United States, 10595

Actively Recruiting

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Research Team

L

Lindsay Baker, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

OTHER

Number of Arms

10

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