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Completed Phase 4 Interventional Accepts healthy volunteers Results available

Value of Urodynamic Evaluation

ClinicalTrials.gov ID: NCT00803959

Public ClinicalTrials.gov record NCT00803959. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 8:31 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized Trial of Urodynamic Testing Before Stress-Incontinence Surgery

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Although no reliable and specific figures are available for the total expenditure on UDS, UDS is commonly performed for patients with urinary incontinence (UI) regardless of gender and age. UDS is typically performed prior to incontinence surgery. Urodynamic studies are expensive, time-consuming, and uncomfortable diagnostic investigations. The 3rd ICI reported insufficient evidence with which to answer the following key research questions related to UDS: 1) Do physicians alter clinical decision-making based on results of UDS?, and 2) Do alterations in clinical decisions made in response to UDS results improve the clinical outcomes?

Study identification

NCT ID
NCT00803959
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Carelon Research
Other
Enrollment
630 participants

Conditions and interventions

Interventions

Other

Eligibility (public fields only)

Age range
21 Years and older
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2008
Primary completion
Nov 30, 2009
Completion
May 31, 2010
Last update posted
Aug 5, 2013

2008 – 2010

United States locations

U.S. sites
10
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35294
University of California San Diego California 92103
Loyola University Medical Center Maywood Illinois 60153
University of Maryland Baltimore Maryland 21201
Oakwood Hospital/Cancer Center Dearborn Michigan 48123
Beaumont Hospital Royal Oak Michigan 48073
University of Pittsburgh Pittsburgh Pennsylvania 15213
University of Texas Southwestern Dallas Texas 75390
University of Texas Health Sciences Center San Antonio Texas 78229-3900
University of Utah Salt Lake City Utah 84132

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00803959, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 5, 2013 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00803959 live on ClinicalTrials.gov.

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