MedTrace Logo

Comparing Voiding Trials After Midurethral Sling for Stress Incontinence

NCT02400034 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 112

Last updated 2016-10-21

No results posted yet for this study

Summary

Urinary incontinence is a prevalent health and quality of life concern affecting almost half of women over the age of 20. Urinary retention (abnormal holding of urine) is a concern of many surgeons who perform midurethral sling surgery. All patients after outpatient midurethral sling or vaginal prolpase surgery must complete a voiding trial if they are to be discharged without a catheter. The purpose of this study is to compare two different types of postoperative voiding trials to determine which leads to less post-operative issues, such as urinary retention requiring catheterization. You are being asked to participate because you are having midurethral sling surgery, either with or without vaginal prolapse repair.

Conditions

  • Stress Urinary Incontinence
  • Urethral Hypermobility
  • Cystocele

Interventions

OTHER

Voiding trial

1 of 2 tests to assess bladder function after midurethral sling surgery with and without anterior or posterior colporrhaphy

Sponsors & Collaborators

  • Northwell Health

    lead OTHER

Principal Investigators

  • Harvey A Winkler, MD · North Shore LIJ Divsion of Female Pelvic Medicine and Reconstructive Surgery

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-03-31
Primary Completion
2016-06-30
Completion
2016-06-30

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02400034 on ClinicalTrials.gov