Value of Urodynamic Evaluation

NCT00803959 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 630

Last updated 2013-08-06

Study results available
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Summary

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?

Conditions

Interventions

OTHER

Office evaluation

Office evaluation

OTHER

UDS

Urodynamics

Sponsors & Collaborators

  • University of Alabama at Birmingham

    collaborator OTHER
  • University of California, San Diego

    collaborator OTHER
  • University of Maryland

    collaborator OTHER
  • University of Pittsburgh

    collaborator OTHER
  • University of Texas Southwestern Medical Center

    collaborator OTHER
  • The University of Texas Health Science Center at San Antonio

    collaborator OTHER
  • University of Utah

    collaborator OTHER
  • Beaumont Hospital

    collaborator OTHER
  • Loyola University

    collaborator OTHER
  • Carelon Research

    lead OTHER

Principal Investigators

  • Ann Gormley, MD · Dartmouth-Hitchcock Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
21 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-11-30
Primary Completion
2009-12-31
Completion
2010-06-30

Countries

  • United States

Study Locations

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Entities

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 NCT00803959 on ClinicalTrials.gov