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Urology Database for Outcomes Research


N/A
18 Years
N/A
Open (Enrolling by invite only)
Both
Incontinence, Prostate Cancer, Interstitial Cystitis, Urinary Retention, Pelvic Organ Prolapse

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Trial Information

Urology Database for Outcomes Research


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.


Inclusion Criteria:



All patients undergoing radical prostatectomy, pelvic organ prolapse repair 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.

Type of Study:

Observational

Study Design:

Observational Model: Case-Only, Time Perspective: Retrospective

Principal Investigator

Kenneth Peters, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

William Beaumont Hospitals

Authority:

United States: Institutional Review Board

Study ID:

2004-050

NCT ID:

NCT00376298

Start Date:

February 2004

Completion Date:

February 2029

Related Keywords:

  • Incontinence
  • Prostate Cancer
  • Interstitial Cystitis
  • Urinary Retention
  • Pelvic Organ Prolapse
  • incontinence
  • prostate cancer
  • interstitial cystitis
  • Cystitis
  • Prolapse
  • Prostatic Neoplasms
  • Urinary Retention
  • Cystitis, Interstitial
  • Pelvic Organ Prolapse

Name

Location
William Beaumont Hospital Royal Oak, Michigan  48073