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Post-operative Dyspareunia clinical trials

View clinical trials related to Post-operative Dyspareunia.

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NCT ID: NCT01299363 Completed - Clinical trials for Post-operative Dyspareunia

Dilators for Dyspareunia Prevention

Start date: September 2010
Phase: Phase 4
Study type: Interventional

This is a randomized clinical trial comparing rates of de novo dyspareunia in women with and without vaginal dilator use following surgery for pelvic organ prolapse with traditional posterior repair. Our hypothesis is daily use of vaginal dilators from post-op week 4 through week 8 after posterior repair will reduce the rate of de novo dyspareunia.