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Prevention of Post Operative Urinary Retention After Thoracic Surgery Trial

Study acronym: PrePOURTS
StatusRecruiting
PhasePhase 2
Started2024-10-01
View on ClinicalTrials.gov ↗
Record status
This record was last updated October 28, 2024 (before its estimated December 30, 2025 completion). Its status may not reflect the trial's current state.

Amendment history

2024-10-24
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v2
Trial statusNot Yet Recruiting→Recruiting
Primary completion date2024-12-30→2025-12-30
Completion date2025-05-31→2026-02-01
Start dateestimated 2024-07-01→confirmed 2024-10-01
Study sitesdetails revised at 1 of 1 site
2024-05-30
Study Identification, Study Status, Study Description, Study Design, Arms and Interventions, Outcome Measures, Eligibility v1
Primary completion date2025-04-30→2024-12-30
Start date2024-04-01→2024-07-01
Enrollment target64→60
Eligibility criteria+619 characters
[...] tion Any known contraindication to the use of tamsulosin HCL Nursing/ Breastfeeding women Use of intraoperative bladder catheter patients for whom cataract and/or glaucoma surgery is scheduled. patients on strong inhibitors of CYP3A4 (e.g., ketoconazole), on moderate inhibitors of CYP3A4 (e.g., erythromycin), on strong (e.g. paroxetine), on moderate (e.g., t [...]
Primary endpoints1 to 3 entries
RateEnrollment ofEffectiveness Monthly postrecruitment Protocol operative urinary retentionadherence
Study description-209 characters
ThisThe objectives of this study willare evaluateto determine the effectivenessfeasibility of providingconducting preoperativea full-scale randomized control trial comparing the efficacy of tamsulosin ascompared prophylaxisto againstplacebo postoperativein reducing post-operative urinary retention afterin people undergoing elective thoracic surgery. ParticipantsPrimary willoutcomes initiatebeing prophylaxismeasured 3are daysthe priorenrollment torate, theirprotocol studyadherence daterate and continueparticipant fordrop 2 days postoperativelyout. This will be a placebo controlled double masked [...]
2024-02-08
Original filing
The objectives of this study are to determine the feasibility of conducting a full-scale randomized control trial comparing the efficacy of tamsulosin compared to placebo in reducing post-operative urinary retention in people undergoing elective thoracic surgery.
Trial Details
NCT Number NCT06262048
Lead Sponsor London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Conditions Urinary Retention Postoperative
Enrollment 60 participants
Start Date 2024-10-01
Primary Completion 2025-12-30 (estimated)
Study Completion 2026-02-01 (estimated)
Updated on ClinicalTrials.gov 2024-10-28