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Assessment of Voiding After Sling

Study:

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

Rationale:

n/a

Purpose:

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.

Study Status: Recruiting

Recruiting:
Geetha Krishnan, RN 216-445-8090 krishng@ccf.org

Geetha Krishnan, RN 216-445-8090 krishng@ccf.org

Condition Intervention Phase
Post-operative Voiding Other: Urinary voiding assessment after midurethral sling N/A

Verified by The Cleveland Clinic August, 2013

Sponsored by: The Cleveland Clinic
Information provided by: The Cleveland Clinic
ClinicalTrials.gov identifier: NCT01343784

Study Type: Interventional

Study Design: Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Screening

Cleveland Clinic Beachwood
Beachwood, Ohio 44122
United States

Cleveland Clinic Hillcrest Hospital
Mayfield Heights, Ohio 44124
United States

John Eric Jelovsek, MD., Principal Investigator
Matthew Barber, MD, MHS., Study Director

This information is abridged to display results relevant only to Cleveland Clinic. To see complete record visit ClinicalTrials.gov
  Information obtained from ClinicalTrials.gov on
Link to the current ClinicalTrials.gov record.

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