60 Participants NeededMy employer runs this trial

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

DJ
Overseen ByDr. John Ademola
Age: 18 - 65
Sex: Female
Trial Phase: Academic
Sponsor: SF Research Institute, Inc.

What You Need to Know Before You Apply

What is the purpose of this trial?

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.

Are You a Good Fit for This Trial?

Inclusion Criteria

1. Women between 20 to 50 years of age.
2. Sexually active, attempting sexual activity, or experiencing concerns related to sexual desire or function, with a partner and have a FSFI total score ≤ 26.55.
3. Have a PSS-10 score of ≥ 14 at screening.
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What Are the Treatments Tested in This Trial?

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Placebo Group

Group I: Shatavari Root Extract (SRI-81) 300 mgExperimental Treatment1 Intervention
Group II: Placebo Capsule (Starch) 300 mgPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

SF Research Institute, Inc.

Lead Sponsor

Trials
7
Recruited
540+

Ixoreal Biomed Private Limited

Industry Sponsor