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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | ashwagandha root | This substance is extracted from the root of the plant. |
| DIETARY_SUPPLEMENT | ashwagandha root and leaf | This substance is extracted from both the root and leaves of the plant. |
| OTHER | Placebo | The 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.