drugset / Trial / NCT03568604

Changes to Vulva, Vestibule, Urethral Meatus and Vagina 20 Weeks Post Daily Prasterone in Women With Dyspareunia

NCT03568604

Phase 4 Completed 18 enrolled San Diego Sexual Medicine
NaSingle-groupOpen-labelTreatment

Summary

Open label study at a single research center. Subjects meeting inclusion and exclusion criteria will receive 6.5 mg prasterone vaginal inserts daily for twenty weeks. A physical examination and vulvoscopy with photography of the vulva, vestibule, urethral meatus and vagina will be performed at baseline and every 4 weeks for 20 weeks. Pain diaries will be completed between visits.

Timeline

Start
2018-08-07
Primary completion
2020-01-28
Completion
2020-01-28

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Dehydroepiandrosterone Other / unclassified 6.5 mg Other

Indications

No indication recorded.