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Clinical Trial Summary

This prospective interventional randomized controlled trial will recruit women with MUI scheduled for surgical treatment where patients will be randomized to either Burch colposuspension, TOT or TVT. Regular postoperative follow up will be planned for at least 2 years. The primary outcome measures will be the objective and subjective cure rates.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02775526
Study type Interventional
Source Ain Shams University
Contact
Status Completed
Phase N/A
Start date May 2016
Completion date January 10, 2020

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