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Local Anesthetic
Pelvic Rehabilitation for Painful Intercourse
Phase 4
Waitlist Available
Led By Mary South, MD
Research Sponsored by University of Cincinnati
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, week 10
Awards & highlights
Study Summary
The purpose of this study is to evaluate which treatment option for pelvic floor pain allows for improved sexual function.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, week 10
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, week 10
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in rating of pain from baseline until the end of the study according to the Iowa Pain Scale
Secondary outcome measures
Change in sexual function between visit 1 and visit 10
Trial Design
2Treatment groups
Active Control
Group I: Pelvic RehabilitationActive Control1 Intervention
Pelvic Rehabilitation will be conduction on weekly basis for a total of 6 weeks
Group II: Trigger Point InjectionsActive Control1 Intervention
Trigger point injections will be administered on weekly basis for a total of 6 weeks
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Who is running the clinical trial?
Patty Brisben Foundation For Women's Sexual HealthOTHER
6 Previous Clinical Trials
359 Total Patients Enrolled
University of CincinnatiLead Sponsor
428 Previous Clinical Trials
634,358 Total Patients Enrolled
Mary South, MDPrincipal InvestigatorUniversity of Cincinnati
Frequently Asked Questions
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