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Urology Database to Evaluate Clinical Information and Improve Patient Care.
This study has been completed.
Sponsored by: William Beaumont Hospitals
Information provided by: William Beaumont Hospitals
ClinicalTrials.gov Identifier: NCT00376298
  Purpose

The purpose of initiating the Urology Database is to evaluate the outcomes of urology procedures and medical management to enhance the care and treatment of urology patients.


Condition
Incontinence
Prostate Cancer
Interstitial Cystitis
Urinary Retention

MedlinePlus related topics: Cancer Interstitial Cystitis Prostate Cancer Urinary Incontinence
U.S. FDA Resources
Study Type: Observational
Study Design: Natural History, Longitudinal, Defined Population, Prospective Study
Official Title: Urology Database for Outcomes Research

Further study details as provided by William Beaumont Hospitals:

Estimated Enrollment: 1000
Study Start Date: February 2004
Estimated Study Completion Date: February 2029
Detailed Description:

The current study population will include all patients having had a radical prostatectomy for the treatment of prostate cancer, as well as patients having had InterStim sacral nerve stimulator implantation beginning January 1, 2002. The database will house data extracted from the medical records. Patient demographics, and preoperative, intra-operative, postoperative, and follow-up clinical data will be collected.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

All patients undergoing radical prostatectomy and InterStim implantation at William Beaumont Hospital beginning January 1, 1998, as well as other urology patients as research questions are identified. Only patients who have accepted William Beaumont Hospital’s Privacy Notices will be included in the database.

Exclusion Criteria:

Patients not acknowledging acceptance of William Beaumont Hospital’s Privacy Notices.

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00376298

Locations
United States, Michigan
William Beaumont Hospital
Royal Oak, Michigan, United States, 48073
Sponsors and Collaborators
William Beaumont Hospitals
Investigators
Principal Investigator: Kenneth Peters, MD William Beaumont Hospitals
  More Information

Study ID Numbers: 2004-050
Study First Received: September 13, 2006
Last Updated: March 6, 2007
ClinicalTrials.gov Identifier: NCT00376298  
Health Authority: United States: Institutional Review Board

Keywords provided by William Beaumont Hospitals:
incontinence
prostate cancer
interstitial cystitis

Study placed in the following topic categories:
Cystocele
Prostatic Diseases
Genital Neoplasms, Male
Urination Disorders
Urinary Bladder Diseases
Cystitis
Urogenital Neoplasms
Urinary Retention
Genital Diseases, Male
Signs and Symptoms
Cystitis, Interstitial
Urologic Diseases
Urinary Incontinence
Prostatic Neoplasms

Additional relevant MeSH terms:
Urological Manifestations
Neoplasms
Neoplasms by Site

ClinicalTrials.gov processed this record on January 15, 2009