Skip to content

Post-Operative Voiding After Gynecological Surgery Trial

Post-Operative Voiding After Gynecological Surgery (POVAGS) Trial: a Randomized Controlled Trial on Retrograde Bladder Filling After Outpatient Gynaecological Laparoscopy

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04198285
Acronym
POVAGS
Enrollment
42
Registered
2019-12-13
Start date
2020-01-10
Completion date
2020-04-27
Last updated
2020-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Complications, Surgery, Urinary Retention

Keywords

laparoscopy, urinary retention

Brief summary

To determine whether partially filling the bladder after outpatient gynaecological laparoscopy expedites time to first void and discharge. Methods: A single site, single-blinded, randomized control trial in which eligible patients undergo partial retrograde bladder filling immediately post-operatively compared to bladder drainage and foley catheter removal. Primary outcome is time to first void, secondary outcomes include time to discharge, post-operative complications and patient satisfaction.

Interventions

PROCEDURERetrograde bladder filling

The bladder will be filled with a large syringe through the urinary catheter (which is left in place for the surgery) with 200mL of sterile saline, and then the catheter will be removed.

Sponsors

Women's College Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Women * Undergoing elective laparoscopy for a gynaecological indication * Plan for same day discharge * Able to provide informed consent

Exclusion criteria

* Pregnancy * Undergoing procedure for pelvic organ prolapse, stress urinary incontinence, or nerve detrapment * Prior hysterectomy, or incontinence/pelvic organ prolapse procedures * Pre-existing voiding dysfunction * Known recurrent urinary tract infections * Known genito-urinary malformations * Known for neuromuscular disorders such as multiple sclerosis * Use of anticholinergic medication * Intraoperative bladder related complications * Need for discharge with indwelling foley catheter * Patients requiring overnight admission for any reason

Design outcomes

Primary

MeasureTime frameDescription
Time to first void3 hoursTime in minutes from arrival in post-operative anesthesia unit (PACU) to first void

Secondary

MeasureTime frameDescription
Time to discharge8 hoursTime in minutes from arrival in PACU to discharge from PACU
Post-operative complications1 week following surgeryUrinary tract infections, or other reported complications
Patient satisfaction1 weekPatients' subjective experience in both groups regarding time spent in PACU and first postoperative week
Post-operative painAssessed at the 1 hour markvisual analogue scale of postoperative pain, assessed in PACU

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026