Urology Database for Outcomes Research - Full Text View

Sponsor:	William Beaumont Hospitals
Information provided by:	William Beaumont Hospitals
ClinicalTrials.gov Identifier:	NCT00444730

Purpose

The purpose of initiating the urology database is to collect relevant retrospective data via chart review related to patients undergoing radical prostatectomy via the retropubic, perineal, laparoscopic, and robotic assisted laparoscopic approaches and InterStim implantation. This data will be utilized to evaluate the health benefits and outcomes of each of these procedures to enhance care and treatment.

Condition	Intervention
Prostate Cancer Pelvic Pain Incontinence	Procedure: Radical Prostatectomy Procedure: InterStim Implantation

Study Type:	Observational
Study Design:	Case Control, Prospective
Official Title:	Urology Database for Outcomes Research

Resource links provided by NLM:

MedlinePlus related topics: Cancer Pelvic Pain Prostate Cancer Urinary Incontinence

U.S. FDA Resources

Further study details as provided by William Beaumont Hospitals:

Biospecimen Retention: None Retained

Biospecimen Description:

Estimated Enrollment:	3000
Study Start Date:	January 2007
Estimated Study Completion Date:	October 2029

Intervention Details:

Surgical procedure for prostate cancer.

surgical placement of the interstim

Detailed Description:

The objective of this study is to initiate and maintain a patient information database that will be used to study the impact of each surgical procedure on patients' overall health, quality of life, and bowel/bladder/sexual function.

The study coordinator will, on an ongoing basis, abstract needed medical information from inpatient hospital and physician office records for inclusion into the database.

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No
Sampling Method:	Non-Probability Sample

Study Population

patients undergoing radical prostatectomy or InterStim implantation at William Beaumont Hospital.

Criteria

Inclusion Criteria:

All patients undergoing radical prostatectomy or InterStim implantation at William Beaumont Hospital.

Exclusion Criteria:

None

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00444730

Contacts

Contact: Kaylyn Petzel, RN

248-551-3565

Locations

United States, Michigan
William Beaumont Hospital	Recruiting
Royal Oak, Michigan, United States, 48073
Contact: Kaylyn Petzel, RN 248-551-3565

Sponsors and Collaborators

William Beaumont Hospitals

Investigators

Principal Investigator:

Kenneth Peters, M.D.

William Beaumont Hospitals

More Information

No publications provided

Responsible Party:	William Beaumont Hospital ( Kenneth Peters )
Study ID Numbers:	2007-031
Study First Received:	March 6, 2007
Last Updated:	May 4, 2009
ClinicalTrials.gov Identifier:	NCT00444730 History of Changes
Health Authority:	United States: Institutional Review Board

Keywords provided by William Beaumont Hospitals:

Prostate Cancer
Prostatectomy
Pelvic pain

urgency
incontinence
frequency

Additional relevant MeSH terms:

Prostatic Diseases
Genital Neoplasms, Male
Urination Disorders
Pain
Urogenital Neoplasms
Genital Diseases, Male
Urological Manifestations

Signs and Symptoms
Neoplasms
Pelvic Pain
Neoplasms by Site
Urologic Diseases
Urinary Incontinence
Prostatic Neoplasms

ClinicalTrials.gov processed this record on November 27, 2009