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Assessment of Voiding After Sling

Assessment of Voiding After Sling (AVAS): A Randomized Trial of Two Methods of Post-operative Catheter Management After Midurethral Sling for Female Stress Urinary Incontinence

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01343784
Acronym
AVAS
Enrollment
105
Registered
2011-04-28
Start date
2011-04-30
Completion date
2013-12-31
Last updated
2014-02-19

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

Conditions

Post-operative Voiding

Keywords

Voiding trial, sling, post-operative assessment, urinary retention

Brief summary

The purpose of this study is to compare the incidence of catheterization from discharge to 6 weeks postoperatively when using two methods of post-operative voiding evaluation after a mid-urethral sling procedure. The investigators' results may lead to a decreased use of indwelling catheters and their associated morbidity after outpatient sling surgery.

Detailed description

Minimally invasive slings have demonstrated similar efficacy to earlier abdominal anti-incontinence procedures, but offer the benefit of shorter operating times, less voiding dysfunction, lower morbidity and are usually done as an outpatient procedure. Despite the advantages, about 35% of patients are discharged home with indwelling catheters. Indwelling catheters are bothersome for patients, costly to the healthcare system and are a source of significant morbidity. The challenge for pelvic surgeons performing anti-incontinence procedures is avoiding postoperative urinary retention while minimizing the use of catheters and their associated risks. A commonly described backfill-assisted voiding trial is used as a means of evaluating bladder function postoperatively. This method uses a low post-void residual as a specific criterion for discharge without a catheter. However, the validity of this method has never been critically evaluated. Our recent observational study suggests that patients may be safely discharged without a catheter after a midurethral sling procedure based on their subjective assessment of the force of stream. Our proposed study expands on this pilot data using a randomized trial to evaluate two methods of post-operative voiding evaluation. The results may lead to a decreased use of indwelling catheters and their associated morbidity after outpatient sling surgery.

Interventions

OTHERUrinary voiding assessment after midurethral sling

Both groups will undergo voiding trial in the similar manner. The decision to discharge based on an objective measure (voided amount) versus based on the subjective measure (force of stream self assessment).

Sponsors

The Cleveland Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 81 Years
Healthy volunteers
No

Inclusion criteria

Enrollment: All patients,18-81 year old, undergoing an outpatient midurethral sling surgery will be screened for participation in the study at the preoperative visit. Exclusion: 1. Women undergoing concomitant urinary tract or pelvic reconstructive procedures 2. Women with pelvic organ prolapse beyond the hymen 3. Women who have undergone a different or same procedure for urinary incontinence in the past 4. Women with neurological conditions, such as multiple sclerosis, spinal cord injury/pathology 5. Cases complicated by a cystotomy or other complication necessitating postoperative catheterization 6. Non-English speakers

Design outcomes

Primary

MeasureTime frameDescription
Total Catheterization RateSurgery to 6-weeks post-operativelyThe incidence of postoperative catheterization (total catheterization) at any point from discharge after surgery to 6 weeks postoperatively. The incidence of being discharged with an indwelling catheter will be gathered from PACU records. The information regarding catheterization after that point will be captured via the electronic medical records or patient questionnaires (at 2 days, 1 week, and 6 week follow-up).

Secondary

MeasureTime frameDescription
Number of return visits to the office or to the emergency room6 weeksThis information will be captured via the EMR or the patient questionnaires, at 2-days, 1-week and 6-weeks folow-up.
Cumulative number of days of catheterization6 weeksCalculated from EMR at the 6-weeks post-operative visit.
Incidence of catheter acquired urinary tract infection (CAUTI)6 weeksUTI is defined according to the CDC as a positive culture \>10\^5 CFU/ml with no more than 2 species of microorganisms in the patient's endorsing 1 or more UTI symptoms.
Time to discharge from PACU30 minutes to 2 hours in recovery roomCollected from EMR.
Subjective assessment of Force of Stream (FOS).30 minutes to 2 hours in recovery roomUsing VAS, the subject compares the post-operative FOS with the pre-operative FOS on a scale of 0-120% given the pre-operative FOS is 100%.
Postoperative pain6 weeksPain scale will be administered at 2-days, 1-week and 6-weeks follow-up.
Patient's expectation of postoperative recoveryAssessed at enrollment, average 10 minutesInformation will be collected via short survey at enrollment. The subject will be asked to assign a level of importance to post-operative factors such as pain control, prolonged catheterization, daily activities and ability to return to work.
Daily function postoperatively as well as satisfaction with the surgery6 weeksInformation will be gathered from questionnaires at 2-days, 1-week and 6-weeks follow-up. Modified validated questionnaire will be used (McCarthy et al).
Effectiveness of the sling procedure6 weeksIncontinence severity index will be collected at enrollment and at 6 weeks post surgery. The score will be compared to determine if the procedure was effective at treating incontinence.

Countries

United States

Outcome results

None listed

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