Trial of Two Techniques to Assess Postoperative Voiding Function
Urinary Retention
About this trial
This is an interventional diagnostic trial for Urinary Retention focused on measuring midurethral sling, voiding study, voiding trial, retrograde voiding trial
Eligibility Criteria
Inclusion Criteria:
- English-speaking
- Women over the age of 18
- Patients with stress urinary incontinence planning to undergo midurethral sling placement
Exclusion Criteria:
- Prior incontinence surgery
- Concomitant surgery for pelvic organ prolapse except for anterior repair
- Intraoperative cystotomy
- Patients taking anticholinergic medication
Sites / Locations
- University of North Carolina
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
OR retrograde fill
PACU retrograde fill
At completion of sling placement in the operating room, the bladder will be filled retrograde via a cystoscope with 300 mL sterile saline or water to inspect for bladder perforation. The cystoscope is removed and the foley catheter is NOT replaced for the duration of the surgery. The surgery is completed and the patient is transferred to the post-anesthesia care unit. Once she is able to ambulate, she will be instructed to void. The voided volume and residual volume will be recorded.
At completion of sling placement in the operating room, the bladder will be filled retrograde via a cystoscope with 300 mL sterile saline or water to inspect for bladder perforation. The cystoscope is removed and the foley catheter is replaced for the duration of the surgery and when complete the patient is transferred to the post-anesthesia care unit. Once she is able to ambulate, she will undergo a retrograde bladder fill with 300 mL of normal saline. The foley catheter will be removed and she will be instructed to void. The voided volume and residual volume will be recorded.