Clinical Trials Directory

Trials / Completed

CompletedNCT07212231

Radicle GI Health: A Study Assessing the Impact of Health and Wellness Products on Gastrointestinal (GI) Health and Related Health Outcomes.

Radicle GI HealthTM RVS: A Randomized, Double-Blind, Placebo-Controlled Direct-to-Consumer Study Assessing the Impact of Health and Wellness Products on Gastrointestinal (GI) Health and Related Health Outcomes.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
1,501 (actual)
Sponsor
Radicle Science · Industry
Sex
All
Age
21 Years – 105 Years
Healthy volunteers
Accepted

Summary

A randomized, double-blind, placebo-controlled study assessing the impact of health and wellness products on GI Health and related health outcomes.

Detailed description

This is a randomized, double-blind, placebo-controlled study conducted with adult participants, residing in the United States. Eligible participants will (1) have the opportunity for meaningful improvement (at least 30%) in their primary health outcome, and (2) express acceptance in taking a product and not knowing its formulation until the end of the study. 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 for 7 weeks. Participant reports of health indicators will be collected at baseline, throughout the active period of study product use, and in a final survey. All study assessments will be electronic; there are no in-person visits or assessments for this real-world evidence study.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTGI Product Placebo ControlParticipants will use their GI Product Placebo Control as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTActive Product 1Participants will use their GI Active Product 1 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTActive Product 2Participants will use their GI Active Product 2 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTActive Product 3Participants will use their GI Active Product 3 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTActive Product 4Participants will use their GI Active Product 4 as directed for a period of 6 weeks.
DIETARY_SUPPLEMENTActive Product 5Participants will use their GI Active Product 5 as directed for a period of 6 weeks.

Timeline

Start date
2025-10-16
Primary completion
2026-03-02
Completion
2026-03-02
First posted
2025-10-08
Last updated
2026-03-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07212231. Inclusion in this directory is not an endorsement.