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Prevention of Post Operative Urinary Retention After Thoracic Surgery Trial — PrePOURTS  

Urinary Retention Postoperative Clinical Trial

Official title:
Prevention of Post Operative Urinary Retention After Thoracic Surgery Trial

Clinical Trial Summary

The objectives of this study are to determine the efficacy of tamsulosin compared to placebo in reducing post-operative urinary retention and improving other clinical outcomes in people undergoing pulmonary surgery.

Clinical Trial Description

This study will evaluate the effectiveness of providing preoperative tamsulosin as prophylaxis against postoperative urinary retention after thoracic surgery. Participants will initiate prophylaxis 3 days prior to their study date and continue for 2 days postoperatively. This will be a placebo controlled double masked randomized trial. The primary outcome being evaluated is development of urinary retention; defined as required urinary catheterization. Secondary outcomes will include rate of straight catheterizations, indwelling catheterizations and time to catheterization. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06262048
Study type Interventional
Source Lawson Health Research Institute
Contact Deb Lewis
Phone 519-685-8500
Email deb.lewis@lhsc.on.ca
Status Not yet recruiting
Phase Phase 2
Start date April 1, 2024
Completion date May 31, 2025
View Details
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