Satavari and Ashoka for Menopause (SAM) Study
Eligible age
40–65 yrs
Accepts
Women
Locations
1 state
Healthy volunteers
No
See if you qualify for this study
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About this study
This 12-week randomized, placebo-controlled clinical trial will evaluate the efficacy and safety of a daily oral supplement containing Ashoka Bark and Shatavari in women experiencing menopausal symptoms. Up to 50 participants will be randomized to receive either the active supplement or placebo, with 40 participants expected to complete the study. Participants will attend visits at Weeks 0, 6, and 12, where hormone levels (FSH and estradiol), menopausal symptoms, quality of life, anxiety, cognitive function, and sleep will be assessed using validated measures. The study will also explore changes in the vaginal microbiome and monitor safety and adherence throughout the trial. The study will be conducted at MusB Research in New Port Richey, Florida.
Sponsor: Vidya USA Corporation
You may qualify if…
- ✓ Females aged 40-65 years.
- ✓ Postmenopausal women in good overall health and fulfilling menopausal criteria set at the MRS score more than 5.
- ✓ Subjects had experienced absence of regular menstrual cycle for at least 3 months.
- ✓ Willingness to sign consent, follow protocols and regimen intake, as well as maintain normal physical activity and follow study procedures.
You may not qualify if…
- ✕ Not on Hormone Replacement Therapy (HRT) or had discontinued HRT at least 12 months before admission to the study.
- ✕ History of breast cancer,
- ✕ BMI ≥ 40mg/kg².
- ✕ Prior removal of both ovaries.
- ✕ Pregnancy, breastfeeding, or plans for pregnancy.
- ✕ History of breast or uterine cancer, including hyperplasia, endometrial carcinoma, or cervical neoplasia.
- ✕ Unstable medical conditions or clinically diagnosed depression requiring treatment.
- ✕ Self-reported drug or alcohol abuse.
Where it's recruiting
New Port Richey
Source: ClinicalTrials.gov · NCT07861295 · last updated 2026-10-06