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Clinical Trial Summary

This study is looking to minimize side effects, while maintaining and potentially improving the therapeutic benefit to patients suffering from Female Sexual Arousal Disorder by providing a topical preparation of Sildenafil locally to the vulvar-vaginal tissue.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04948151
Study type Interventional
Source Strategic Science & Technologies, LLC
Contact Kathy Cornell
Phone 774-473-4414
Email kcornell@strategicscience.com
Status Recruiting
Phase Phase 2
Start date June 28, 2021
Completion date December 15, 2021

See also
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Completed NCT02958176 - Heart Rate Variability Biofeedback for Female Sexual Arousal Disorder N/A
Terminated NCT00572377 - Alprostadil (FemLife Gel) in the Treatment of Female Sexual Arousal Disorder Phase 1
Completed NCT01382719 - Bremelanotide in Premenopausal Women With Female Sexual Arousal Disorder and/or Hypoactive Sexual Desire Disorder Phase 2
Completed NCT05685407 - Examining Caffeine as a Treatment for Antidepressant-induced Arousal Dysfunction in Women Phase 1
Terminated NCT03682601 - Sexual Penetration Pain in Postmenopausal Women: A Topical Botanical Drug Treatment Phase 2
Completed NCT01803802 - Effects of Early Abuse on Adult Intimate Relationships N/A
Completed NCT00640458 - Study to Investigate Effect of Sildenafil on Clitoral Engorgement as Measured by Magnetic Resonance Imaging (MRI) in Pre-menopausal Women With Female Sexual Arousal Disorder Phase 2
Not yet recruiting NCT06116045 - Evaluation of the Efficacy, Safety and Tolerability of BZ371A in Women With Sexual Arousal Disorder Phase 2