Status:
TERMINATED
Incontinence Ring on Stress Urinary Incontinence
Lead Sponsor:
Queen's University
Collaborating Sponsors:
The Physicians' Services Incorporated Foundation
Conditions:
Stress Urinary Incontinence
Urinary Incontinence
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
This study aims as defining success rate of the incontinence ring in women with test proven stress urinary incontinence and determining factors associated with successful use.
Detailed Description
The primary objective of this study is to determine if the incontinence ring is effective in decreasing the incontinence episode frequency per week. Other objectives include the determination of the c...
Eligibility Criteria
Inclusion
- Symptoms of urinary stress urinary incontinence (i.e. urinary leakage associated with increased intra-abdominal pressure/cough) (if mixed incontinence the urinary stress urinary incontinence symptoms must predominate)
- Urodynamic Stress urinary incontinence confirmed by urodynamic studies (i.e. urinary leakage associated with increased intra-abdominal pressure/cough in the absence of detrusor overactivity)
- Ability to understand spoken and written English
Exclusion
- Severe pelvic organ prolapse (\> or = stage 3 on the Pelvic Organ Prolapse Quantification System - POP-Q)
- Contraindications to pessary use (including acute vaginal/urinary or pelvic infections, vaginal or cervical lesions or unexplained vaginal bleeding)
- Inability to properly fit the incontinence ring
Key Trial Info
Start Date :
June 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2008
Estimated Enrollment :
29 Patients enrolled
Trial Details
Trial ID
NCT00427778
Start Date
June 1 2006
End Date
May 1 2008
Last Update
September 27 2017
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Kingston General Hospital
Kingston, Ontario, Canada, K7L2V7