Void Trials After Two Voiding Trials (TVT)

Withdrawn before enrolling · Not applicable

Conditions studied: Postoperative Voiding Dysfunction, Postoperative Urinary Retention

In brief

The primary objective of this project is to compare the rate of postoperative voiding dysfunction in two voiding trials (the retrograde-fill technique versus the spontaneous-fill technique) after midurethral sling (MUS) procedures with tension-free vaginal tape (TVT) without any concomitant surgery.

Key facts

Study ID

NCT03937531

Run by

Icahn School of Medicine at Mount Sinai

People needed

0

Starts

2020-02-01

Expected to finish

2022-05-30

Last updated by the study team

2020-04-28

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Any adult female (age >= 18 years old) undergoing an outpatient TVT surgery for SUI will be eligible for participation.
• Participants must be able to provide informed consent and complete all study requirements.

You may not qualify if…

• Participants will be excluded if the surgery involves any concomitant urinary tract or pelvic reconstructive procedure or if the procedure, in itself, necessitates PUC, as in the event of a cystotomy, bladder perforation or intraoperative hemorrhage
• Participants with a history of neurologic conditions affecting the urinary tract system, POP beyond the hymen during straining (any compartment), or previous anti-incontinence procedure will be also excluded.

Where it is running

• Mount Sinai West — New York, New York, United States
• Mount Sinai Medical Center — New York, New York, United States

Full record on ClinicalTrials.gov

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