A Clinical Evaluation of the Tension-Free Vaginal Tape Obturator System For Treatment of Stress Urinary Incontinence (Urinary Leakage)

Completed · Not applicable

Conditions studied: Stress Urinary Incontinence

In brief

Stress urinary incontinence affects nearly 30 million women worldwide and the main goal of surgical treatment is to stop urinary incontinence (urinary leakage) that occurs with physical activity, coughing, sneezing, etc.Patients in the study will have an operation to improve urinary incontinence symptoms. This will involve inserting a mesh sling to help support the urethra (tube leading into your bladder). During the operation, the study doctor will use tension-free vaginal obturator system. The study will include women diagnosed with Stress Urinary Incontinence who have completed their families.

Key facts

Study ID

NCT00196521

Run by

Ethicon, Inc.

People needed

300

Starts

2005-01-01

Expected to finish

2007-03-01

Last updated by the study team

2007-12-13

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Patient has objective demonstrable signs of stress urinary incontinence (SUI), including patients with ISD. Objective testing includes: standing stress test, urodynamics evaluation, or pad test.
• Patient is age 18 or older.
• Patient had a hysterectomy, tubal ligation or is otherwise incapable of pregnancy, or had a negative pregnancy test prior to study entry and has decided to cease childbearing.
• Patient agrees to participate in the study, including completion of all study-related procedures and evaluations, and documents this agreement by signing the IRB/EC-approved informed consent.

You may not qualify if…

• Patient has an associated or suspected neurological disease.
• Patient is on anti-coagulation therapy.
• Patient has received an investigational drug or device in the past 60 days.
• For patients having URP measurements at selected sites:
• Patient has an active lesion or present injury to perineum or urethra.Patient has a urethral obstruction.
• Patient has an unreduced cystocele > Stage 1. (Reduction of prolapse prior to URP testing is required.) Reduction of Cystocele (if applicable). Patients should be seated in a semi-fowler's position with head of bed at 40-60 degrees.
• Carefully place a half of a speculum into the vagina, reducing prolapse to less than stage 1. Be careful not to over extend or elongate the vaginal length.
• The half of a speculum must be placed with pressure emphasis on the posterior and apical areas. Anterior wall pressure or urethral pressure must be avoided at all times.
• The subject has active infection upon urine dipstick analysis, defined as ≥+1 leukocytes or ≥+1 nitrates (Must reschedule appointment after UTI resolves.)

Where it is running

• Urogynecology Associates of CO — Denver, Colorado, United States
• Bladder Control Center — Norwalk, Connecticut, United States
• Urogynecology Specialists of Kenuckiana — Louisville, Kentucky, United States
• Greater Baltimore Medical Center — Baltimore, Maryland, United States
• Oakwood Hospital — Dearborn, Michigan, United States
• Sheldon Freedman, MD — Las Vegas, Nevada, United States
• St. Peter's University Hospital — New Brunswick, New Jersey, United States
• The Institute for Female Pelvic Medicine & Reconstructive Surgery — Allentown, Pennsylvania, United States
• University Urology — Knoxville, Tennessee, United States
• McDonlad Murrmann Women's Clinic — Memphis, Tennessee, United States
• Sound Urology Ambulatory Surgery Center — Edmonds, Washington, United States
• Sunnybrook & Women's College Health Sciences Center — Toronto, Ontario, Canada
• Service d'Urologie — Marseille, France
• Hopital Des Diaconesses — Paris, France
• Klinikum der Eberhard-Karls-Universität — Tübingen, Germany
• Women's and Children's Hospital — Singapore, Singapore
• Samsung Medical Center — Seoul, South Korea
• University of Ulsan College of Medicine and Asan Medical Center — Seoul, South Korea
• Southport District General Hospital — Southport, United Kingdom

Full record on ClinicalTrials.gov

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