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NCT06524674 · ClinicalTrials.gov registry record · NA
Clinical Study to Compare the Effect of an Oral Rehydration Solution on the Rate of Absorption of Functional Ingredients
A NA study, sponsored by Liquid I.V..
- Completed
- Registry status
- NA
- Development phase
- 37
- Enrollment target
NCT06524674 is a NA study that has completed, run by Liquid I.V.. The registered enrollment target is 37 participants.
The verdict
NCT06524674, a NA study, has completed, sponsored by Liquid I.V..
- COMPLETED
- Registry status
- NA
- Development phase
- 37 participants
- Enrollment target
Study Summary
The objective of this study was to compare the individual pharmacokinetics of functional ingredients included in an oral rehydration solution (ORS) with or without the inclusion of active base ingredients (carbohydrate and electrolytes). The functional ingredients included in both the control and test solutions were Melatonin in conjunction with L-theanine (Arm 1), Caffeine in conjunction with L-theanine (Arm 2), and Vitamin C in conjunction with Zinc (Arm 3), across two study periods. The primary outcomes of this study included the relative pharmacokinetics of each functional ingredient. These included: maximum observed concentration (C max), time of maximum observed concentration (T max), cumulative Area Under the Curve (AUC) for each timepoint, (including AUC from the time of dosing to the time of last observation) and the concentration at each timepoint for the corresponding functional ingredients included in the specific study arm (i.e., melatonin, L-theanine, caffeine, vitamin C and zinc).
Interventions
- DIETARY_SUPPLEMENT Hydration Multiplier + Energy
- DIETARY_SUPPLEMENT Hydration Multiplier + Sleep
- DIETARY_SUPPLEMENT Energy Comp
- OTHER Sleep Comp
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 37 participants |
| Start Date | 2023-10-01 |
| Est. Completion | 2024-05-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06524674
The ClinicalTrials.gov registry entry for NCT06524674 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 37 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Liquid I.V., which has 5 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 4 interventions - of which Hydration Multiplier + Energy is the first listed.
NCT06524674 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT06524674 about?
NCT06524674 is a clinical study titled "Clinical Study to Compare the Effect of an Oral Rehydration Solution on the Rate of Absorption of Functional Ingredients". The objective of this study was to compare the individual pharmacokinetics of functional ingredients included in an oral rehydration solution (ORS) with or without the inclusion of active base ingredients (carbohydrate and electrolytes). The functional ingredients included in both the control and te...
What is the current status of trial NCT06524674?
This trial is currently completed. It is a NA study. The enrollment target is 37 participants. The study started on 2023-10-01. Estimated completion is 2024-05-31.
What interventions are being tested in trial NCT06524674?
The interventions under investigation include: Hydration Multiplier + Energy (DIETARY_SUPPLEMENT), Hydration Multiplier + Sleep (DIETARY_SUPPLEMENT), Energy Comp (DIETARY_SUPPLEMENT), Sleep Comp (OTHER).
Who is sponsoring clinical trial NCT06524674?
This trial is sponsored by Liquid I.V., which has 5 total clinical trials registered on ClinicalTrials.gov.
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