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Radicle Women's Health DNS™: A Study Assessing the Impact of Health and Wellness Products on Fatigue and Related Women's Health Outcomes

NCT07735247 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 550

Last updated 2026-07-29

No results posted yet for this study

Summary

Radicle Women's Health DNSTM: A randomized, double-blind, placebo-controlled direct-to-consumer study assessing the impact of health and wellness products on fatigue and related women's health outcomes

Conditions

Interventions

DIETARY_SUPPLEMENT

Placebo Health Control Product

Participants will use their Placebo Health Control Product as directed for a period of 8 weeks

DIETARY_SUPPLEMENT

Active Health Product

Participants will use their Active Health Product as directed for a period of 8 weeks

Sponsors & Collaborators

  • Radicle Science

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-07-14
Primary Completion
2027-07-14
Completion
2027-07-14

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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 NCT07735247 on ClinicalTrials.gov