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RECRUITING NA

Clinical Study to Evaluate the Effects of Two Novel Hydration Beverage Formulas on Rehydration in Healthy Adults

NCT05428228 · View on ClinicalTrials.gov ↗

Study Summary

The aim of the clinical trial is to evaluate the efficacy of two novel hydration products on rehydration following exercise.

Interventions

  • OTHER Placebo
  • OTHER TP1
  • OTHER TP2

Study Locations (1)

Tennessee

  • The University of Memphis — Memphis

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2022-10-01
Est. Completion 2024-09-01
Phase NA

Sponsor

Liquid I.V.

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05428228

The ClinicalTrials.gov registry entry for NCT05428228 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 16 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Liquid I.V., which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 5 conditions, with Dehydration appearing as the primary indexed condition, and to 3 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05428228 reports 1 study location spanning 1 distinct geographic area — top geographies include Tennessee. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05428228 about?

NCT05428228 is a clinical study titled "Clinical Study to Evaluate the Effects of Two Novel Hydration Beverage Formulas on Rehydration in Healthy Adults". The aim of the clinical trial is to evaluate the efficacy of two novel hydration products on rehydration following exercise.

What is the current status of trial NCT05428228?

This trial is currently recruiting. It is a NA study. The enrollment target is 16 participants. The study started on 2022-10-01. Estimated completion is 2024-09-01.

What conditions does trial NCT05428228 study?

This clinical trial studies the following conditions: Dehydration, Exercise Performance, Cognitive Performance, Exercise Recovery, Rehydration. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05428228?

The interventions under investigation include: Placebo (OTHER), TP1 (OTHER), TP2 (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05428228?

This trial is sponsored by Liquid I.V., which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05428228 being conducted?

This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial