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Outcomes Comparison of Robotic, Retropubic, and Perineal Prostatectomy

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00442000
First Posted: March 1, 2007
Last Update Posted: March 21, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
William Beaumont Hospitals
  Purpose
Compare peri-operative and postoperative outcomes of the three different surgical approaches to prostatectomy

Condition Intervention
Prostate Cancer Procedure: Prostatectomy

Study Type: Observational
Study Design: Time Perspective: Retrospective
Official Title: Outcomes Comparison of Robotic, Retropubic, and Perineal Prostatectomy

Resource links provided by NLM:


Further study details as provided by William Beaumont Hospitals:

Enrollment: 700
Study Start Date: January 2005
Study Completion Date: December 2009
Primary Completion Date: December 2009 (Final data collection date for primary outcome measure)
Intervention Details:
    Procedure: Prostatectomy
    Patients undergoing prostatectomy.
Detailed Description:
Existing data collected from Prostatectomy Database study and Urology Database study will be analyzed. Compare peri-operative and postoperative outcomes of the three different surgical approaches to prostatectomy
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients undergoing prostatectomy at William Beaumont-Royal Oak.
Criteria

Inclusion Criteria:

  • 18 years of age
  • Radical Prostatectomy at William Beaumont Hospital

Exclusion Criteria:

  • Dementia
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00442000


Locations
United States, Michigan
William Beaumont Hospital
Royal Oak, Michigan, United States, 48073
Sponsors and Collaborators
William Beaumont Hospitals
Investigators
Principal Investigator: Kevin Feber, M.D. William Beaumont Hospitals
  More Information

Responsible Party: William Beaumont Hospitals
ClinicalTrials.gov Identifier: NCT00442000     History of Changes
Other Study ID Numbers: E2007-024
First Submitted: February 28, 2007
First Posted: March 1, 2007
Last Update Posted: March 21, 2012
Last Verified: March 2012

Keywords provided by William Beaumont Hospitals:
Prostate Cancer
Prostatectomy

Additional relevant MeSH terms:
Prostatic Neoplasms
Genital Neoplasms, Male
Urogenital Neoplasms
Neoplasms by Site
Neoplasms
Genital Diseases, Male
Prostatic Diseases