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Radicle Relief 24_RLN: A Study Assessing the Impact of Health and Wellness Products on Pain and Related Health Outcomes.

NCT07160712 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1000

Last updated 2025-12-11

No results posted yet for this study

Summary

A randomized, double-blind, placebo-controlled direct-to-consumer study assessing the impact of health and wellness products on pain and related health outcomes.

Conditions

Interventions

DIETARY_SUPPLEMENT

Relief Product Placebo Control

Participants will use their Relief Product Control as directed for a period of 6 weeks.

DIETARY_SUPPLEMENT

Relief Active Product 1

Participants will use their Relief Active Product 1 as directed for a period of 6 weeks.

DIETARY_SUPPLEMENT

Relief Active Product 2

Participants will use their Relief Active Product 2 as directed for a period of 6 weeks.

DIETARY_SUPPLEMENT

Relief Active Product 3

Participants will use their Relief Active Product 3 as directed for a period of 6 weeks.

Sponsors & Collaborators

  • Radicle Science

    lead INDUSTRY

Principal Investigators

  • Susan Hewlings · Radicle Science

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
105 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-09-04
Primary Completion
2025-12-08
Completion
2025-12-08

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07160712 on ClinicalTrials.gov