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Clinical Trial Summary

The purpose of this study is to determine if perineorrhaphy performed with surgical vaginal prolapse repair improves sexual function.


Clinical Trial Description

The decision to include perineorrhaphy into vaginal prolapse repair is made solely on surgeon preference and personal experience. Little research has been done to explore the short-term and long-term post-operative consequences of perineorrhaphy. This study will explore the effects of perineorrhaphy on post-op sexual function.

Subjects will be randomized to receive a perineorrhaphy in conjunction with their surgical vaginal prolapse repair or to have the surgical repair performed without a perineorrhaphy. At the 6-8 week post op visit, subjects will be asked questions about the presence of genital pain. Subjects will then be given validated symptom and quality of life study questionnaires at 6 and 12 month post op visits to assess sexual function.

Subject partners will be invited to participate after the participant has finalized informed consent. If partner decides to participate, they will complete the a partner questionnaire. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03333811
Study type Interventional
Source Wake Forest University Health Sciences
Contact Candace Parker-Autry, MD
Phone 336-716-3779
Email cparkera@wakehealth.edu
Status Not yet recruiting
Phase N/A
Start date February 2018
Completion date June 2018

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