Pre-operative Tamsulosin and Time to Spontaneous Void After Hysterectomy
- Registration Number
- NCT04859660
- Lead Sponsor
- University of Arizona
- Brief Summary
The aim of this study is to determine if a one time dose of tamsulosin given pre-operatively decreases the time to void and the time to discharge after minimally invasive hysterectomy.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 161
- Women 18-80 undergoing outpatient minimally invasive hysterectomy
- Inability to provide informed consent
- Bladder malignancy
- Intra-operative bladder or ureteral injury; anticipated prolonged bladder catheterization
- Plan for sling or anterior repair
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Tamsulosin- intervention group Tamsulosin - Placebo group Placebo -
- Primary Outcome Measures
Name Time Method Time to Spontaneous Void 8 weeks Each participant underwent a void trial post-operatively by backfilling their bladder with 200cc normal saline at the conclusion of the case and removing the foley. Patients needed to void at least 100cc to be considered to have "passed" their void trial.
- Secondary Outcome Measures
Name Time Method Time to Discharge From the Post-anesthesia Care Unit 8 weeks The time from the patient leaving the OR to the time they were discharged home from the Post-anesthesia care unit was recorded to determine the Time to discharge.
Trial Locations
- Locations (2)
Banner University Medical Center- Phoenix
🇺🇸Phoenix, Arizona, United States
Banner University Medical Center- Tucson
🇺🇸Tucson, Arizona, United States