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Clinical Trial Summary

After incontinence surgery, the patients randomly will be divided two groups. In group A postoperative urinary catheterization time will be applied one day, In group B catheterization will be applied two days. After removal of urinary catheter, residual volume will be measured and voiding function will be controlled. In postoperative period; third, sixth month and one year after surgery stress test will be applied to control success of surgery


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03225742
Study type Observational
Source Kanuni Sultan Suleyman Training and Research Hospital
Contact
Status Completed
Phase
Start date February 1, 2017
Completion date February 1, 2018

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