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COMPLETEDNA

Oral Rehydration Solution in Healthy Adults

Effects of Oral Rehydration Solution on Dehydration Recovery in Adults

NCT06130475•Abbott Nutrition

Summary

This is a prospective, randomized, controlled, blinded, crossover study to evaluate the effects of an oral hydration solution.

Eligibility

Age

18 - 40 years

Sex

ALL

Healthy Volunteers

Yes

Inclusion Criteria

•Participant is 18 to 40 years of age.
•Participant has a body mass index (BMI) ≥ 18 and ≤ 30 kg/m2
•Participant reports having a moderate to heavy sweat rate when physically exerted or in extreme heat
•Participant is male or non-pregnant, non-lactating female, at least 6 weeks postpartum prior to screening visit.
•Participant has a systolic blood pressure \<130 mm Hg and a diastolic blood pressure \< 90 mm Hg without the use of anti-hypertensive medications.
•Participant reports no predisposing cardiovascular conditions.
•If female, participant has a regular menstrual cycle
•Participant is willing to consume grape-flavored beverages during the study.
•If participant is on chronic medication the dosage must be constant for at least 2 months prior to enrollment and able to maintain medication, type and dose throughout duration of study
•Participant is weight-stable for the two months prior to screening visit
+4 more criteria

Exclusion Criteria

•Participant is a current or recent (the past 8 weeks) participant in a weight-conscious sport such as but not limited to wrestling, powerlifting, boxing, rowing, gymnastics or any martial arts, with participation defined as ≥ 3x weekly training
•Participant is currently, and for the past 4 weeks or longer: running \>40 miles per week on average, cycling \>80 miles per week on average or swimming \>20,000 yards per week on average
•Participant is participating in another study that has not been approved as a concomitant study
•Participant has used a sauna in the past 4 weeks
•Participant uses any form of tobacco or nicotine, or other controlled substance not prescribed by a physician
•Participant has previous history with heat illness or injury that resulted in a visit to a medical center in the past 12 months
•Participant has an eating disorder, severe dementia or delirium, history of significant neurological or psychiatric disorder, alcoholism, substance abuse or other conditions that may interfere with study product consumption or compliance with study protocol procedures
•Participant is currently taking or has taken antibiotics within 6 weeks of enrollment
•Participant is currently taking or has taken a diuretic within 1 week of enrollment
•Participant has been diagnosed with the following:
+6 more criteria

Locations (1)

University of Central Florida

Orlando, Florida, United States

Key Dates

Start Date

March 15, 2024

Primary Completion Date

December 16, 2024

Completion Date

December 16, 2024

Last Updated

January 14, 2025

Enrollment

ACTUAL participants

Conditions

Dehydration

Interventions

Oral Rehydration Solution (ORS)

OTHER

Water

OTHER

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: January 14, 2025Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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Oral Rehydration Solution in Healthy Adults

Inclusion Criteria

Exclusion Criteria

Point of Care Ultrasound and Co-loading in Patients With Spinal-induced Hypotension and Cardiac Diseases

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Effect of a Mobile-Based Hydration Tracking Program on Knowledge, Attitudes, and Behaviors in Older Adults