TVT-SECUR A Pilot Study for the Treatment of Stress Urinary Incontinence

Completed

Conditions studied: Stress Urinary Incontinence

In brief

The primary objective of this study is to obtain clinical performance information on the GYNECARE TVT-SECUR\* System (Tension-free Support for Incontinence) in women with stress urinary incontinence (SUI).

Key facts

Study ID

NCT00463554

Run by

Ethicon, Inc.

People needed

72

Starts

2006-04-01

Expected to finish

2007-12-01

Last updated by the study team

2023-08-23

Who can join

Age: 21 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Must be female with objective, demonstratable signs of SUI or stress predominant mixed incontinence and requires elective, primary surgical intervention.
• Must be at least 21 years old.
• Must be postmenopausal (amenorrhea) for at least 1 year or surgically sterile (bilateral salpingo-oophorectomy or tubal ligation or otherwise be incapable of pregnancy) or has a negative pregnancy test prior to study entry and has decided to cease childbearing.
• Agrees to participate in the study, including all study related procedures and evaluations and documents this agreement by signing the IRB/EC-approved informed consent

You may not qualify if…

• Have any other coexistent pathology requiring concomitant surgery that may impact this procedure i.e. surgeries that involve the anterior vaginal wall (e.g. anterior colporrhaphy, diverticula, anterior Prolift) Any allowable concomitant surgery must be performed prior to the GYNECARE TVT SECUR System surgery.
• Have intrinsic sphincter deficiency (ISD) [Urethral Pressure Profile (UPP) with a maximum urethral closing pressure (MUCP) < 20cm H2O or Leak Point Pressure (LPP) < 60].
• Have an active urinary tract infection (UTI) or vaginal infection at time of surgery.
• Have a fixed urethra (< 30° mobility on Q-Tip Straining Test).
• Have had prior incontinence surgery.
• Have a post-void residual volume > 100mL.
• Have co-existent pelvic organ prolapse that is symptomatic or extends beyond the hymen.
• Have lower urinary tract pathology in the form of a fistula or diverticulum.
• Have a malignancy or with a history of malignancy within the past 5 years, except for a basal cell carcinoma that has been treated with local excision and is no longer present.
• Are on anticoagulant therapy.
• Have received an experimental drug or used an experimental medical device within 30 days prior to the planned start of treatment.
• Are deemed by the investigator as medically unfit for surgery or who in the opinion of the investigator should not be enrolled in the study because of the precautions, warnings or contraindications outlined in the GYNECARE TVT SECUR System IFU.
• Employees of the investigator or study center with direct involvement in the proposed study or other studies under the direction of that investigator or study center.

Where it is running

• Michigan Institute of Women's Health — Dearborn, Michigan, United States
• Good Samaritan Hospital — Cincinnati, Ohio, United States
• The Institute for Female Pelvic Medicine and Reconstructive Surgery — Allentown, Pennsylvania, United States
• Vanderbilt University — Nashville, Tennessee, United States
• Helsinki University Central Hospital — Helsinki, Finland
• University of Padova — Padova, Italy

Full record on ClinicalTrials.gov

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