drugset / Trial / NCT05968937

Vaginal Baclofen Suppositories in Chronic Pelvic Pain

NCT05968937

Phase 2 Completed 39 enrolled University of Louisville
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate if baclofen vaginal suppositories improve symptoms of Chronic Pelvic Pain (CPP). Participants in this study will take four short questionnaires prior to being randomized. Randomization is like flipping a coin; participants have an equal likelihood of being randomized to the treatment group (vaginal baclofen suppositories) or placebo group (vaginal suppository without baclofen ingredient). Participants will take their assigned treatment nightly for 8 weeks. Follow up visits will be at the 4 and 8 week time frames, when questionnaires will again be completed. Participants may receive additional treatments for CPP during the course of the study. After 8 weeks Participants will be offered a prescription for baclofen suppositories and the study drug will be stopped. Follow up on patient symptoms with questionnaires will again occur at 12 weeks.

Timeline

Start
2024-01-01
Primary completion
2026-01-01
Completion
2026-01-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Baclofen Small molecule 20 mg Other

Indications