Urology Database to Evaluate Clinical Information and Improve Patient Care.

Sponsor
Kenneth Peters, MD (Other)
Overall Status
Completed
CT.gov ID
NCT00376298
Collaborator
William Beaumont Hospitals (Other)
215
1
142
1.5

Study Details

Study Description

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.

Study Design

Study Type:
Observational
Actual Enrollment :
215 participants
Observational Model:
Case-Only
Time Perspective:
Retrospective
Official Title:
Urology Database for Outcomes Research
Study Start Date :
Feb 1, 2004
Actual Primary Completion Date :
Dec 1, 2015
Actual Study Completion Date :
Dec 1, 2015

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 William Beaumont Hospital Royal Oak Michigan United States 48073

    Sponsors and Collaborators

    • Kenneth Peters, MD
    • William Beaumont Hospitals

    Investigators

    • Principal Investigator: Kenneth Peters, MD, William Beaumont Hospitals

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Kenneth Peters, MD, Principal Investigator, William Beaumont Hospitals
    ClinicalTrials.gov Identifier:
    NCT00376298
    Other Study ID Numbers:
    • 2004-050
    First Posted:
    Sep 14, 2006
    Last Update Posted:
    Dec 24, 2015
    Last Verified:
    Dec 1, 2015
    Keywords provided by Kenneth Peters, MD, Principal Investigator, William Beaumont Hospitals
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 24, 2015