Clinical Trials Directory

Trials / Terminated

TerminatedNCT04994431

Post-Operative Urinary Retention (POUR) in Thoracic Surgery Patients Receiving Prophylactic Tamsulosin

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
109 (actual)
Sponsor
University of Massachusetts, Worcester · Academic / Other
Sex
Male
Age
60 Years
Healthy volunteers
Not accepted

Summary

Post-Operative Urinary Retention (POUR) in Thoracic Surgery is a prospective interventional study aiming to test the hypothesis that the prophylactic use of tamsulosin prior to thoracic surgery in high risk patients leads to reduce the rates of POUR.

Detailed description

Post-operative urinary retention (POUR) is one of the most common post-operative complications encountered by most surgical specialties. The incidence of POUR can vary from five to 70%. Post-operative urinary retention is a prevalent complication. Patients who undergo thoracic surgery have greater urinary retention rates compared to others. Data on effective methods to reduce the risk of POUR in this high-risk group are limited. All subjects who meet inclusion and exclusion criteria will be invited to participate. There will be no randomization. All will receive tamsulosin in the pre operative period.

Conditions

Interventions

TypeNameDescription
DRUGTamsulosin Hydrochloride0.4mg orally nightly for the two days immediately prior to surgery and the morning of surgery.

Timeline

Start date
2021-08-01
Primary completion
2023-10-04
Completion
2023-10-04
First posted
2021-08-06
Last updated
2024-11-07
Results posted
2024-11-07

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04994431. Inclusion in this directory is not an endorsement.