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A Randomized Trial Comparing Horizontal and Vertical Vaginal Cuff Closure

Hysterectomy Clinical Trial

Official title:
A Randomized Trial Comparing Horizontal and Vertical Vaginal Cuff Closure

Clinical Trial Summary

The purpose of this study is to evaluate the possible impacts of two techniques of vaginal cuff closure during robotic hysterectomy. We aim to compare vertical vs horizontal vaginal cuff closure and the impact that these techniques have on vaginal length, sexual function, and overall complication rates.

Clinical Trial Description

A Validated questionnaire the Female Sexual Function Index (FSFI) and total vaginal lengths will be used to evaluate patients pre-operatively, at 4-6 weeks post-operatively, and 6 months post operatively. The FSFI will also be sent to the patient 12 months post operatively. These data will be used to assess sexual function and total vaginal length in patients undergoing minimally invasive hysterectomy. The study endpoint will occur after the 12 month follow-up questionnaire. Additionally, all complications following surgery will be tracked over the study period for comparison. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02117492
Study type Interventional
Source Milton S. Hershey Medical Center
Contact
Status Completed
Phase N/A
Start date May 2014
Completion date May 2017
View Details
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