Status:
UNKNOWN
Optimization of Spontaneous Postoperative Trial of Void Among Women
Lead Sponsor:
Women and Infants Hospital of Rhode Island
Collaborating Sponsors:
American Urogynecologic Society
American Association of Gynecologic Laparoscopists
Conditions:
Urinary Retention Postoperative
Voiding Disorders
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
Trial of void (TOV) is a diagnostic test performed on all women who undergo prolapse repair or incontinence surgery, due to the importance of diagnosing postoperative urinary retention (POUR). Inciden...
Detailed Description
Patients will learn to perform self-catheterization ('clean intermittent catheterization', or CIC) preoperatively; after surgery, the investigators will collect a range of voiding parameters used duri...
Eligibility Criteria
Inclusion
- English-speaking women, age \>18yo
- Scheduled for urogynecology procedure which will need post-operative trial of void (including pelvic organ prolapse and/or stress urinary incontinence repair), with plan for same-day discharge.
Exclusion
- Unable or unwilling to perform self-catheterizatoin either by patient or willing family member
- Pre-existing voiding dysfunction defined as documented PVR \> 200 mL
- Intraoperative urinary tract injury needing indwelling catheter on discharge
- Need for overnight admission
Key Trial Info
Start Date :
September 10 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 30 2021
Estimated Enrollment :
183 Patients enrolled
Trial Details
Trial ID
NCT04010656
Start Date
September 10 2018
End Date
December 30 2021
Last Update
July 20 2021
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Women & Infants Hospital
Providence, Rhode Island, United States, 02903