Post Operative Urinary Retention (POUR) Following Thoracic Oncological Surgery

Recruiting Early Phase 1 Interventional Study
Urinary Retention
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
55 and older
Sex
Male
Trial phase
Early Phase 1
Study type
Interventional
Purpose
Prevention
Participants needed
46 (estimated)
Sponsor
Hackensack Meridian Health · Other
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About This Trial

This is a feasibility study looking at whether the use of Tamsulosin could lower the high incidence of postoperative urinary retention (POUR) in older men who undergo an oncological thoracic surgical procedure for suspected or confirmed cancer. In addition, the study will try to identify the time of resumption of presurgical urinary function post Tamsulosin administration.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Males * ≥55 years old * Planned thoracic oncological surgical procedure of a video assisted oncological surgical procedure for suspected or confirmed cancer. * Surgery scheduled more than 7 days from the time of consent Exclusion Criteria: * Using Tamsulosin already * Known …
Contacts

Denise Theiler, RN

7327763301

Denise.Theiler@hmhn.org

CONTACT