Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07210229

The Effectiveness of a Proprietary Ashwagandha Extract on Menopausal Symptoms: A Three-Arm Randomized, Double-Blinded, Placebo Controlled Clinical Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
90 (estimated)
Sponsor
Nutraceuticals Research Institute · Academic / Other
Sex
Female
Age
40 Years – 55 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the efficacy of two proprietary ashwagandha extracts on symptoms of menopause and hormone levels, as compared to a placebo.

Detailed description

Participants will take one of two extracts or a placebo every day for 84 days; outcomes of self-report menopausal symptoms collected on a trio of scales will provide information on effectiveness.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTashwagandha rootThis substance is extracted from the root of the plant.
DIETARY_SUPPLEMENTashwagandha root and leafThis substance is extracted from both the root and leaves of the plant.
OTHERPlaceboThe inert placebo does not contain any of the plant matter.

Timeline

Start date
2025-10-01
Primary completion
2026-02-28
Completion
2026-03-30
First posted
2025-10-07
Last updated
2025-10-07

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07210229. Inclusion in this directory is not an endorsement.