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

NCT07210229 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2025-10-07

No results posted yet for this study

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.

Conditions

  • Menopausal Hot Flashes
  • Menopausal Women

Interventions

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.

Sponsors & Collaborators

  • Nutraceuticals Research Institute

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-10-01
Primary Completion
2026-02-28
Completion
2026-03-30

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 NCT07210229 on ClinicalTrials.gov