Urology Database to Evaluate Clinical Information and Improve Patient Care.

Prostate Cancer Clinical Trial

Official title:

Urology Database for Outcomes Research

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00376298
• Other study ID #: 2004-050
• Status: Completed
• Phase: N/A
• First received: September 13, 2006
• Last updated: December 22, 2015
• Start date: February 2004
• Est. completion date: December 2015

Study information

• Verified date: December 2015
• Source: William Beaumont Hospitals
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 215
• Est. completion date: December 2015
• Est. primary completion date: December 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

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.

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Cystitis
• Cystitis, Interstitial
• Incontinence
• Interstitial Cystitis
• Pelvic Organ Prolapse
• Prostate Cancer
• Prostatic Neoplasms
• Urinary Retention

Locations

Country	Name	City	State
United States	William Beaumont Hospital	Royal Oak	Michigan

Sponsors (2)

Lead Sponsor	Collaborator
Kenneth Peters, MD	William Beaumont Hospitals

Country where clinical trial is conducted

United States,