Trigger Point Injections and Pelvic Rehabilitation for the Treatment of Pelvic Floor Myalgia and Sexual Pain

Status unconfirmed · Phase 4

Conditions studied: Dyspareunia

In brief

The purpose of this study is to evaluate which treatment option for pelvic floor pain allows for improved sexual function.

Key facts

Study ID

NCT02022722

Run by

University of Cincinnati

People needed

36

Starts

2013-08-01

Expected to finish

2014-06-01

Last updated by the study team

2013-12-30

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• pelvic pain
• pelvic floor myalgia
• dyspareunia
• female
• age > 18 years

You may not qualify if…

• interstitial cystitis
• vaginal lesions / ulcerations
• prior trigger point injections in the past 6 months
• prior pelvic rehabilitation in the past 6 months
• laparoscopically documented endometriosis / pelvic adhesions or adhesive disease
• documented pelvic inflammatory disease identified within the past 6 months
• documented sexually transmitted disease within the past 6 months

Where it is running

• Division of Urogynecology, University of Cincinnati Medical Center — Cincinnati, Ohio, United States (enrolling)

Full record on ClinicalTrials.gov

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