San Francisco, CANCT07441083Now EnrollingIRB Ready

Sexual Wellness Clinical Trial in San Francisco, CA

Access cutting-edge sexual wellness treatment through this clinical trial at a research site in San Francisco. Study-provided care at no cost to qualified participants.

Sponsored by SF Research Institute, Inc.

Quick Self-Assessment

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Preparing your pre-screening questions…

Expert Care in San Francisco

Access sexual wellness specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related sexual wellness treatment provided free

Apply for This San Francisco Location

Check if you qualify for this sexual wellness clinical trial in San Francisco, CA

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to San Francisco

    Convenient for CA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit San Francisco site if eligible
  4. 4Begin participation

About This Sexual Wellness Study in San Francisco

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.

Sponsor: SF Research Institute, Inc.

Who Can Participate

Inclusion Criteria

Women between 20 to 50 years of age.
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.
Have a PSS-10 score of ≥ 14 at screening.
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.).
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.
Participants having sufficient understanding to communicate effectively with the investigator and are willing to discuss their sexual functioning with the investigative staff.
Able to read and write in English or any other vernacular language.
No plan to commence new treatments over the study period.
Must have the ability and willingness to sign a written informed consent and to comply with all study procedures.

Exclusion Criteria

Participants taking any form of herbal extract in the last 3 months before study entry.
Participants with hormonal imbalance including PCOS, and symptoms of perimenopause and menopause
Participants who are on hormone replacement therapy (HRT) for more than 3 months.
Participants with any active medical, surgical, or gynaecological problems.
Participants with a history of alcohol, tobacco dependence, or any other substance abuse
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.
Participants with mental condition rendering the subject unable to understand the nature, scope, and possible consequences of the study.
Participants with demonstrated inability to comply with the study procedures, including poor compliance.
Participants with inability to attend follow-up visits.
Patients with known hypersensitivity to Shatavari, or any of the ingredients of study interventions.
Patients who had participated in other clinical trials during the previous 3 months.
Patients who have any clinical condition, according to the investigator who does not allow safe fulfilment of clinical trial protocol.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in San Francisco?

Yes, this clinical trial (NCT07441083) has an active research site in San Francisco, CA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Sexual Wellness Treatment Options in San Francisco, CA

If you're searching for sexual wellness treatment options in San Francisco, CA, this clinical trial (NCT07441083) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our San Francisco research site is actively enrolling participants for this clinical trial. You'll receive care from experienced sexual wellness specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all sexual wellness clinical trials near you to find additional studies recruiting in your area.

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