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OpenTrials
Completed

NCT Number: NCT00453739

TVT Worldwide Registry

The objective of this observational study is to obtain long -term clinical and patient reported outcomes on the use of the GYNECARE family of TVT (Tension-Free Vaginal Tape) systems in women with stress urinary incontinence.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

The Townsville Hospital Department of Urogynaecology, Douglas, Australia

Loading trial locations.

About this study

Sites may include patients with either the GYNECARE TVT SECUR System, GYNECARE TVT System, or the GYNECARE TVT Obturator System

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women diagnosed with SUI who are suitable candidates for a TVT system, as according the relevant Instructions for Use (IFU).

Treatment and study plan

Primary outcomes

  1. Standing cough stress test

    Time frame: 12 months

Secondary outcomes

  1. I-QOL score

    Time frame: 3, 6, 12 and 24 months

Sponsors and collaborators

Lead sponsor

Ethicon, Inc.

Industry

Registry information

Official study title

TVT-World Wide Observational Registry for Long-Term Data

Important dates

Study start
2007
Primary completion
2010
Study completion
2010
First posted
Mar 29, 2007
Registry last updated
May 6, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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