Precise Transvaginal Tape Placement Trial

Completed · Not applicable

Conditions studied: Stress Urinary Incontinence, Urinary Incontinence

In brief

This purpose of this study is to study is to see if intra-operative urethral length measurement with the Foley catheter will improve the placement of a synthetic sling in the mid-urethra.

Key facts

Study ID

NCT02101489

Run by

Loyola University

People needed

56

Starts

2014-03-01

Expected to finish

2016-11-01

Last updated by the study team

2017-03-01

Who can join

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

You may qualify if…

• Candidates for TVT
• >=18 years of age to participate

You may not qualify if…

• Inability to give informed consent
• Previous SUI(stress urinary incontinence) treatment including TVT, Burch or urethral bulking agents
• Previous bladder, urethral malignancies or vaginal/pelvic radiation treatment.
• Pregnant women cannot participate

Where it is running

• Loyola University Health System — Maywood, Illinois, United States

Full record on ClinicalTrials.gov

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