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Preoperative Tamsulosin to Prevent Postoperative Urinary Retention After Surgery For Pelvic Floor Disorders

Urinary Retention Clinical Trial

Official title:
Preoperative Tamsulosin to Prevent Postoperative Urinary Retention in Females After Surgery For Pelvic Floor Disorders

Clinical Trial Summary

Our hypothesis is that patients receiving preoperative Tamsulosin will have decrease rates of postoperative urinary retention (POUR) after surgery in females for pelvic floor disorders.

Clinical Trial Description

This study is a prospective randomized control trial. Patients undergoing pelvic surgery will randomized into two groups. The study group will receive one oral dose of .4mg of Tamsulosin preoperatively.The control group will receive one placebo pill preoperatively. Success or failure of initial voiding trial in postoperative period will be measured. Patients who fail the voiding trial will be discharged home with Foley catheter as is standard protocol at our institution. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04232683
Study type Interventional
Source The Cleveland Clinic
Contact
Status Active, not recruiting
Phase Early Phase 1
Start date December 18, 2019
Completion date June 2024
View Details
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