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Vaginal Tactile Imaging for the Assessment of Pelvic Organ Prolapse Repair Efficiency

Pelvic Organ Prolapse Clinical Trial

Official title:
Vaginal Elasticity Assessment Before and After the Affect of Surgical Repair for Pelvic Organ Prolapse (POP) on Vaginal Elasticity as Measured by Vaginal Tactile Imaging

Clinical Trial Summary

Female patients with POP will be evaluated for vaginal elasticity using vaginal tactile imaging both before and after surgery for the repair of the POP. Surgical repair will be performed by a single surgeon who will perform either a laparoscopic or vaginal repair.

Clinical Trial Description

Patients will be recruited and sign a consent form. The patients included are patients with POP that are candidates for either laparoscopic or vaginal 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

Clinical Trial Details
NCT number NCT03311685
Study type Interventional
Source Rambam Health Care Campus
Contact
Status Completed
Phase N/A
Start date August 1, 2018
Completion date July 20, 2020
View Details
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