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Radicle Relief RAL™: A Study Assessing the Impact of Health and Wellness Products on Pain Relief and Related Health Outcomes

NCT07262775 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 715

Last updated 2026-04-21

No results posted yet for this study

Summary

Radicle Relief RAL: A randomized, double-blind, placebo-controlled study assessing the impact of health and wellness products on pain relief and related health outcomes.

Conditions

  • Pain Interference

Interventions

DIETARY_SUPPLEMENT

Pain Relief Supplement Product Placebo Control

Participants will use their Pain Relief Supplement Product Placebo Control as directed for a period of 8 weeks

DIETARY_SUPPLEMENT

Pain Relief Supplement Active Product 1

Participants will use their Pain Relief Supplement Active Product 1 as directed for a period of 8 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
2025-12-18
Primary Completion
2027-01-04
Completion
2027-01-04

Countries

  • United States

Study Locations

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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 NCT07262775 on ClinicalTrials.gov