Post Operative Urinary Retention (POUR) Following Thoracic Oncological Surgery

Trial statusRecruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexMale
Age55+
SponsorHackensack Meridian Health

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.

Eligibility criteria

Qualifiers

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

Disqualifiers

Using Tamsulosin already

Known allergy to Tamsulosin or sulfa drugs

Current use of Boceprevir

Resting systolic blood pressure <100

Trial design

Treatments tested in this trial

  • Tamsulosin

Treatment groups

46 Participants
are divided into 1 treatment group

Sponsors and collaborators