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Clinical Trial Summary

Female patients with USI will be evaluated for vaginal elasticity using vaginal tactile imaging both before and after surgery for the repair of the USI. Surgical repair will be performed by a single surgeon who will perform a tension free vaginal tape obturator (TVT-O) repair.


Clinical Trial Description

Patients will be recruited and sign a consent form. The patients included are patients with USI that are candidates for a TVT-O repair.

Assessment of vaginal elasticity via vaginal tactile imaging will be performed at 3 different points:

- The day of surgery before surgery.

- The day after surgery.

- 3 months post-operational. Every patient will serve as her own control. Demographic, gynecologic and obstetric history will be obtained from patients` electronic files. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03301818
Study type Interventional
Source Rambam Health Care Campus
Contact
Status Completed
Phase N/A
Start date August 1, 2018
Completion date July 20, 2020

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