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NCT05111392 · ClinicalTrials.gov registry record · Phase 1

Hydration Dynamics and Influence of Beverage Composition

A Phase 1 study, sponsored by University of Illinois at Chicago.

Completed
Registry status
Phase 1
Development phase
14
Enrollment target

NCT05111392: Completed Phase 1 study, sponsored by University of Illinois at Chicago.

NCT05111392 is a Phase 1 study that has completed, run by University of Illinois at Chicago. The registered enrollment target is 14 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05111392, a Phase 1 study, has completed, sponsored by University of Illinois at Chicago.

COMPLETED
Registry status
Phase 1
Development phase
14 participants
Enrollment target

Study Summary

The study examines interactions between fluid availability in the gut and fluid retention in the body. The relative rate of fluid uptake, the expansion of the plasma volume, and percent of fluid retained by the body will be measured in response to ingestion of beverages of different composition. Healthy, euhydrated adults will be studied. The results will help establish formulations of beverages that sustain if not promote acute euhydration.

Primary Outcome

Measure the rate of fluid uptake by the gut using appearance of deuterium oxide, or D2O, in the blood after ingesting a fixed volume of placebo.

Interventions

  • BIOLOGICAL Placebo
  • BIOLOGICAL Oral Rehydration Solution 1
  • BIOLOGICAL Oral Rehydration Solution 2

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2021-09-03
Est. Completion 2022-11-30
Phase Phase 1
University of Illinois at Chicago

430 total trials

What the finished NCT05111392 record still lists

NCT05111392 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 14 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (77% lower).

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT05111392 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05111392 about?

NCT05111392 is a clinical study titled "Hydration Dynamics and Influence of Beverage Composition". The study examines interactions between fluid availability in the gut and fluid retention in the body. The relative rate of fluid uptake, the expansion of the plasma volume, and percent of fluid retained by the body will be measured in response to ingestion of beverages of different composition. Hea...

What is the current status of trial NCT05111392?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 14 participants. The study started on 2021-09-03. Estimated completion is 2022-11-30.

What interventions are being tested in trial NCT05111392?

The interventions under investigation include: Placebo (BIOLOGICAL), Oral Rehydration Solution 1 (BIOLOGICAL), Oral Rehydration Solution 2 (BIOLOGICAL).

Who is sponsoring clinical trial NCT05111392?

This trial is sponsored by University of Illinois at Chicago, which has 430 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05111392's enrollment target sits among peer trials

14 1844th of 2000 higher than 154 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05111392, the US trial registry maintained by the National Library of Medicine. NCT05111392 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.