Urology Database for Outcomes Research
1 other identifier
observational
860
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2007
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2007
CompletedFirst Submitted
Initial submission to the registry
March 6, 2007
CompletedFirst Posted
Study publicly available on registry
March 8, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2014
CompletedAugust 28, 2014
August 1, 2014
7.6 years
March 6, 2007
August 26, 2014
Conditions
Keywords
Interventions
Surgical procedure for prostate cancer.
Surgical pelvic organ prolapse repair
Eligibility Criteria
patients undergoing radical prostatectomy or InterStim implantation at William Beaumont Hospital.
You may qualify if:
- All patients undergoing radical prostatectomy or InterStim implantation at William Beaumont Hospital.
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Kenneth Peters, MDlead
- Corewell Health Eastcollaborator
Study Sites (1)
William Beaumont Hospital
Royal Oak, Michigan, 48073, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Kenneth Peters, M.D.
Corewell Health East
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
March 6, 2007
First Posted
March 8, 2007
Study Start
January 1, 2007
Primary Completion
August 1, 2014
Study Completion
August 1, 2014
Last Updated
August 28, 2014
Record last verified: 2014-08