Clinical Trials Directory

Trials / Completed

CompletedNCT06981468

Hydration To be Optimized (H2O) With a Low-sodium Beverage

H2O - Hydration to be Optimized With a Low-sodium Beverage

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
43 (actual)
Sponsor
Société des Produits Nestlé (SPN) · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

In this study, the investigators want to assess the effects of a new beverage containing whey protein and glycerol (two different dosages) on hydration status in healthy adults when compared to the control (water). This is a single-center, double-blinded, 3 arm cross-over randomized controlled study looking to enroll 45 healthy adult participants. The study will be performed at the Clinical Innovation Lab (CIL), Nestlé Research, Lausanne. Participants will be screened and randomly assigned to 1 of 6 sequences of consumption. Enrolled participants will have three visit days. They will consume one of the test products, or control at each visit and complete the study assessments.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLow Sodium Beverage 1The first interventional product for this study is a low-sodium beverage containing Dose 1 of glycerol, whey protein, and water. It will come in a ready to drink format for the participants.
DIETARY_SUPPLEMENTLow Sodium Beverage 2The second interventional product for this study is a low-sodium beverage containing dose 2 of glycerol, whey protein, and water. It will come in a ready to drink format for the participants.
OTHERControl (placebo) groupWater

Timeline

Start date
2025-04-16
Primary completion
2025-06-30
Completion
2025-06-30
First posted
2025-05-20
Last updated
2025-11-28

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT06981468. Inclusion in this directory is not an endorsement.