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Not Yet RecruitingNCT07206979

An Open Label Trial Assessing the Impact of a Hydration Formula on Overall Health

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
660 (estimated)
Sponsor
Radicle Science · Industry
Sex
All
Age
21 Years – 105 Years
Healthy volunteers
Accepted

Summary

An Open Label Trial Assessing the Impact of a Hydration Formula on Overall Health

Detailed description

This is an open label study conducted with adult participants residing in the United States. Eligible participants will (1) agree to consume a hydration product, (2) agree not to take any other hydration or electrolyte supplements for the duration of the trial, (3) be 21 years of age or older, and (4) agree to participate in this study for 2 week and answer assessments. Participants that report a known cardiac dysfunction, liver or kidney disease may be excluded. Participants that report a known contraindication or with well-established, significant safety concerns due to illness will be excluded. Heavy drinkers and those who report they are pregnant, trying to become pregnant, or breastfeeding will be excluded. Participants that report taking medications with a known contraindication or with well-established, significant safety concerns will be excluded. Self-reported data are collected electronically from eligible participants over 2 weeks. Participant reports of health indicators will be collected at screening and throughout the active period of study product use. All study assessments will be electronic; there are no in-person visits or assessments for this real-world evidence study.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTHydration Active Product 1Participants will use their Hydration Active Product 1 as directed for a period of 1 week.
DIETARY_SUPPLEMENTHydration Active Product 2Participants will use their Hydration Active Product 2 as directed for a period of 1 week.
DIETARY_SUPPLEMENTHydration Active Product 3Participants will use their Hydration Active Product 3 as directed for a period of 1 week.

Timeline

Start date
2025-09-30
Primary completion
2026-09-30
Completion
2026-09-30
First posted
2025-10-03
Last updated
2025-10-03

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07206979. Inclusion in this directory is not an endorsement.