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

SF Research Institute, Inc.

Status: Enrolling

Conditions: Women Health; Sexual Wellness

Treatments: Dietary Supplement: Shatavari (Asparagus racemosus) Root Extract; Other: Placebo Capsule

Study type: Interventional

Funder types: NETWORK; Industry

Identifiers

NCT07441083

Ixo/2025/1314/SHT/SexWel/GB/01

Details and patient eligibility

About

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.

Full description

Women's sexual wellness is influenced by biological, psychological, and social factors. Stress and neuroendocrine imbalance play a central role in sexual dysfunction and distress. Shatavari (Asparagus racemosus), a traditional Ayurvedic herb, has been historically used to support female reproductive health, hormonal balance, and stress modulation.

This multi-national, prospective, randomized, double-blind, parallel-group study will enroll women aged 20 to 50 years in India and the United States. Eligible participants with reduced sexual function and elevated perceived stress will be randomized in a 1:1 ratio to receive either SRI-81 Shatavari root extract (300 mg/day) or a matched placebo for 12 weeks.

Efficacy will be primarily assessed using the Female Sexual Function Index (FSFI). Secondary outcomes include sexual distress, sexual satisfaction, perceived stress, quality of life, salivary cortisol measures, and laboratory safety parameters. Safety will be evaluated through adverse event monitoring and laboratory investigations.

Enrollment: 60 estimated patients

Sex: Female

Ages: 20 to 50 years old

Volunteers: Accepts Healthy Volunteers

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.
4. Women presenting with signs and symptoms suggestive of stress (e.g., difficulty, concentrating, physical exhaustion, anxiety, restlessness, insomnia, headache, fatigue, loss of appetite, worry, sweating, mental confusion, etc.).
5. Participants who are reliable, honest, compliant, and agree to co operate with all trial evaluations as well as to be able to perform them as per investigator's opinion.
6. Participants having sufficient understanding to communicate effectively with the investigator and are willing to discuss their sexual functioning with the investigative staff.
7. Able to read and write in English or any other vernacular language.
8. No plan to commence new treatments over the study period.
9. Must have the ability and willingness to sign a written informed consent and to comply with all study procedures.

Exclusion criteria

1. Participants taking any form of herbal extract in the last 3 months before study entry.
2. Participants with hormonal imbalance including PCOS, and symptoms of perimenopause and menopause
3. Participants who are on hormone replacement therapy (HRT) for more than 3 months.
4. Participants with any active medical, surgical, or gynaecological problems.
5. Participants with a history of alcohol, tobacco dependence, or any other substance abuse
6. Participants with clinically relevant cardiovascular, gastrointestinal, hepatic, neurologic, endocrine, haematologic or other major systemic diseases making implementation of the protocol or other interpretation of the study result difficult.
7. Participants with mental condition rendering the subject unable to understand the nature, scope, and possible consequences of the study.
8. Participants with demonstrated inability to comply with the study procedures, including poor compliance.
9. Participants with inability to attend follow-up visits.
10. Patients with known hypersensitivity to Shatavari, or any of the ingredients of study interventions.
11. Patients who had participated in other clinical trials during the previous 3 months.
12. Patients who have any clinical condition, according to the investigator who does not allow safe fulfilment of clinical trial protocol.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

---

60 participants in 2 patient groups, including a placebo group

Shatavari Root Extract (SRI-81) 300 mg

Experimental group

Description:

Participants randomized to this arm will receive a standardized Shatavari (Asparagus racemosus) root extract (SRI-81) capsule containing 300 mg, administered orally once daily after breakfast with water for a duration of 12 weeks. The intervention is intended to evaluate the efficacy and safety of Shatavari root extract in improving women's sexual wellness, including sexual function, sexual distress, sexual satisfaction, perceived stress, quality of life, and physiological stress markers, compared with placebo.

Treatment:

Dietary Supplement: Shatavari (Asparagus racemosus) Root Extract

Placebo Capsule (Starch) 300 mg

Placebo Comparator group

Description:

Participants randomized to this arm will receive an identical placebo capsule containing 300 mg of starch, administered orally once daily after breakfast with water for 12 weeks. The placebo is matched in appearance, color, and packaging to the active intervention to maintain blinding. This arm serves as the comparator for evaluating the efficacy and safety of Shatavari root extract in women's sexual wellness.

Treatment:

Other: Placebo Capsule