Sponsor:
Center for Vulvovaginal Disorders
Code:
NCT03189238
Conditions
Female Orgasmic Disorder
Eligibility Criteria
Sex: Female
Age: 25 - 50
Healthy Volunteers: Not accepted
Interventions
Peri-urethral and clitoral injections
Brief summary:
Conditions
Female Orgasmic Disorder
Study ID
NCT03189238
Start date
Jun 28, 2017
Status verified date
Jun, 2017
Completion date
Jul, 2019
Anticipated
Primary completion date
May, 2019
Anticipated
Eligibility Criteria
Sex: Female
Age: 25 - 50
Healthy Volunteers: Not accepted
Enrollment
40 participants
Anticipated
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary purpose
Treatment
Arms
placebo comparator: Placebo
active comparator: PRP
Interventions
Peri-urethral and clitoral injections
Primary outcome measure
Central contacts
The Centers for Vulvovaginal Disorders
(202) 887-0568Locations
The Center for Vulvovaginal Disorders
Recruiting
Washington, D.C., District of Columbia, United States, 20037
Contacts
Andrew T Goldstein, MD
202-887-0568Sponsor
Center for Vulvovaginal Disorders
Last update posted
Jun 26, 2017
Last verified
Jun, 2017
Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Center for Vulvovaginal Disorders on 2017-06-26.