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Void Trials After Two Voiding Trials (TVT)

NCT03937531 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2020-04-28

No results posted yet for this study

Summary

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.

Conditions

  • Postoperative Voiding Dysfunction
  • Postoperative Urinary Retention

Interventions

PROCEDURE

Bladder Scanner

PVR will be measured by using a bladder scanner.

Sponsors & Collaborators

Principal Investigators

  • Woojin Chong, MD · Icahn School of Medicine at Mount Sinai

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-02-29
Primary Completion
2021-05-30
Completion
2022-05-30

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03937531 on ClinicalTrials.gov