Recruiting
Phase 2

Baclofen

Sponsor:

University of Louisville

Code:

NCT05968937

Conditions

Chronic Pelvic Pain Syndrome

Eligibility Criteria

Sex: Female

Age: 18 - 65

Healthy Volunteers: Accepted

Interventions

20 mg baclofen vaginal suppository daily per vagina

Placebo

Study Details

Eligibility Criteria

Study Design

Interventions and Outcome Measures

Central Contacts and Locations

More Information

Trial information was received from ClinicalTrials.gov and was last updated on 2025-06-16. This information was provided to ClinicalTrials.gov by University of Louisville on 2025-02-20.