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Clinical Trials/NCT00376298
NCT00376298
Completed
Not Applicable

Urology Database for Outcomes Research

Kenneth Peters, MD1 site in 1 country215 target enrollmentFebruary 2004

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Incontinence
Sponsor
Kenneth Peters, MD
Enrollment
215
Locations
1
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

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.

Detailed Description

The current study population will include all patients having had a radical prostatectomy for the treatment of prostate cancer, surgical prolapse repair as well as patients having had InterStim sacral nerve stimulator implantation. 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.

Registry
clinicaltrials.gov
Start Date
February 2004
End Date
December 2015
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor Investigator
Principal Investigator

Kenneth Peters, MD

Principal Investigator

William Beaumont Hospitals

Eligibility Criteria

Inclusion Criteria

  • All patients undergoing radical prostatectomy, pelvic organ prolapse repair and neurostimulator (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.

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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