Completed

Effects of Novel Electrolyte Beverages on Rehydration in Healthy Adults

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What is being tested

Test product 1

+ Test product 2

+ Placebo

Other
Who is being recruted

From 18 to 35 Years
+2 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Basic Science Study

Placebo-Controlled
Interventional
Study Start: August 2022
See protocol details

Summary

Principal SponsorLiquid I.V.
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: August 1, 2022

Actual date on which the first participant was enrolled.

This study focuses on the effects of different oral rehydration solutions on the hydration status of healthy adult males. Dehydration can significantly impact both physical and mental performance, especially in hot conditions or after prolonged exercise. The study aims to address the challenge of restoring water and electrolyte balance after activities that cause sweating. Two novel hydration beverages are being tested, both of which are electrolyte drink mixtures containing five essential vitamins and three times more electrolytes than typical sports drinks. These beverages are designed to supply water to the bloodstream earlier in the digestive system, potentially improving rehydration efficiency. The study's importance lies in its potential to improve understanding of how these beverages can aid rehydration, ultimately enhancing recovery after physical exertion. During this study, participants will consume the test beverages. The study is designed as a randomized, placebo-controlled, semi-blind, crossover study, meaning some participants will receive a placebo, and the order of beverage consumption will vary among participants. The study will measure the effectiveness of the beverages through two primary methods: the beverage hydration index and urine specific gravity analysis. The beverage hydration index is a measure of how well a drink hydrates the body, while urine specific gravity analysis provides information about the body's hydration status. By evaluating these measures, the study aims to understand the impact of these beverages on rehydration.

Official TitleEfficacy of Different Oral Rehydration Solutions on the Hydration Status of Healthy Males
Principal SponsorLiquid I.V.
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

15 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Basic Science Study

Basic science studies help researchers understand how the body works or how a disease develops. They don't test treatments, but they build the foundation for future therapies.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Male

Biological sex of participants that are eligible to enroll.

From 18 to 35 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

1 inclusion criteria required to participate
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.

1 exclusion criteria prevent from participating
A history or presence of a clinically relevant cardiac, renal, hepatic, endocrine (including diabetes mellitus), pulmonary, biliary, gastrointestinal, pancreatic, or neurologic disorder. Consumption other nutritional supplements, performance enhancing drugs, and non-steroidal anti-inflammatory drugs (NSAIDs) during the clinical. Participant has any medical condition which alters fluid balance in the body as confirmed by a health history questionnaire. Following a dietary pattern which may alter our findings (e.g., low carbohydrate/ketogenic diet, carnivore diet, intermittent fasting etc.). Women are excluded due to the variability of fluid retention during the menstrual cycle. Participant is not currently enrolled in another clinical study. Participant is consuming any medication which may alter fluid retention such as diuretics. The participant is an employee of the Sponsor.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

3 intervention groups are designated in this study

33.333% chance of being blinded to the placebo group

Treatment Groups

Group I

Experimental
Participants will consume test product 1 during one experimental visit.

Group II

Experimental
Participants will consume test product 2 during one experimental visit.

Group III

Placebo
Participants will consume placebo during one experimental visit.

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Lipscomb University

Nashville, United StatesOpen Lipscomb University in Google Maps
CompletedOne Study Center