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Ambulatory Urodynamic Evaluation of Sacral Neuromodulation for Non-Obstructive Urinary Retention

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified September 2009 by Maastricht University Medical Center.
Recruitment status was:  Enrolling by invitation
Sponsor:
ClinicalTrials.gov Identifier:
NCT00970242
First Posted: September 2, 2009
Last Update Posted: September 4, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Maastricht University Medical Center
  Purpose
Ambulatory Urodynamic measurement on patients with diminished or absent bladder contractility before and after trial with Sacral Neuromodulation therapy.

Condition
Acontractile Bladder

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Ambulatory Urodynamic Evaluation of Sacral Neuromodulation for Non-obstructive Urinary Retention

Further study details as provided by Maastricht University Medical Center:

Estimated Enrollment: 25
Study Start Date: August 2009
Estimated Study Completion Date: January 2012
Estimated Primary Completion Date: January 2012 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients with diminished or absent bladder contraction
Criteria

Inclusion Criteria:

  • Patients with diminished or absent bladder contraction

Exclusion Criteria:

  • Prior Neuromodulation therapy
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00970242


Locations
Netherlands
MaastrichtUMC
Maastricht, Netherlands
Sponsors and Collaborators
Maastricht University Medical Center
Investigators
Principal Investigator: Sajjad Rahnama'i, MD Maastricht University Medical Center
  More Information

Responsible Party: Sajjad Rahnama'i, department of Urology
ClinicalTrials.gov Identifier: NCT00970242     History of Changes
Other Study ID Numbers: MEC 09-4-053
First Submitted: September 1, 2009
First Posted: September 2, 2009
Last Update Posted: September 4, 2009
Last Verified: September 2009

Additional relevant MeSH terms:
Urinary Retention
Urination Disorders
Urologic Diseases