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Clinical Trial Summary

The study aims to evaluate the efficacy of prophylactic tamsulosin in reducing the incidence of postoperative urinary retention in primary total knee and hip arthroplasty patients.


Clinical Trial Description

Prophylactic administration of tamsulosin will be compared to a placebo to evaluate the effectiveness in reducing the incidence of postoperative urinary retention in total hip and knee arthroplasty patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02518971
Study type Interventional
Source University of Michigan
Contact
Status Terminated
Phase Phase 3
Start date August 2015
Completion date December 19, 2018

See also
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