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Study identifier: NCT07441083 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy and Safety of Shatavari Root Extract in Women's Sexual Wellness

Condition: Sexual Wellness · Women Health  ·  Sponsor: SF Research Institute, Inc.

PhaseNA
Planned participants60
Who can joinFemale, 20 Years to 50 Years
Healthy volunteersYes

About this study

This randomized, double-blind, placebo-controlled clinical study is designed to evaluate the efficacy and safety of a standardized Shatavari (Asparagus racemosus) root extract (SRI-81) in improving women's sexual wellness. Sexual wellness is assessed as a multidimensional construct encompassing sexual function, sexual distress, sexual satisfaction, perceived stress, quality of life, and physiological stress markers. Participants will receive either Shatavari root extract or placebo for 12 weeks, with assessments conducted at baseline and follow-up visits.

This description comes directly from the study's public registry record.

Talk to the study team

Dr. John Ademola  ·  415-845-4638  ·  jademola@sfinstitute.com

Always discuss trial participation with your own doctor first.

Locations (1)

San Francisco Research InstituteSan Francisco, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07441083