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Clinical Trials/NCT01643954
NCT01643954
Active, Not Recruiting
N/A

Retrospective/Prospective Analysis of Surgical Outcomes of Robotic Prostatectomy at Ohio State University/The James.

Ohio State University Comprehensive Cancer Center1 site in 1 country1,531 target enrollmentSeptember 23, 2008
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ConditionsProstate Cancer

Overview

Phase
N/A
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
Ohio State University Comprehensive Cancer Center
Enrollment
1531
Locations
1
Primary Endpoint
Collect and analyze descriptive characteristics of patient population and summarize patient outcome data.
Status
Active, Not Recruiting
Last Updated
4 months ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

This is a retrospective/prospective Analysis of surgical outcomes of robotic prostatectomy.

Detailed Description

This retrospective / prospective study will allow us to collect and analyze the presurgical, peri-operative, and outcome data of patients who undergo robotic radical prostatectomy at The Arthur G. James Cancer Hospital and Solove Research Institute, The Ohio State University Medical Center, beginning February 2008 onwards.

Registry
clinicaltrials.gov
Start Date
September 23, 2008
End Date
July 31, 2027
Last Updated
4 months ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Steven Clinton

Principal Investigator

Ohio State University Comprehensive Cancer Center

Eligibility Criteria

Inclusion Criteria

  • •Patients with prostate cancer who have undergone robotic radical prostatectomy at The Arthur G. James Cancer Hospital and Solove Research Institute, The Ohio State University Medical Center.
  • •Ability to understand and willingness to sign the written informed consent document.
  • •18 years and older
  • •Inclusion Criteria:
  • •Patients with prostate cancer that will undergo robotic radical prostatectomy at The Arthur G. James Cancer Hospital and Solove Research Institute, The Ohio State University Medical Center.
  • •Ability to understand and willingness to sign the written informed consent document.
  • •18 years and older

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Collect and analyze descriptive characteristics of patient population and summarize patient outcome data.

Time Frame: up to 20 years

Secondary Outcomes

  • Determine the overall survival(up to 20 years)
  • Correlate the patient characteristics to the surgical outcomes.(up to 20 years)
  • Determine the rate of local recurrence in patients undergoing robotic prostatectomy and compare these metrics to historical controls.(up to 20 years)
  • disease- free survival(up to 20 years)

Study Sites (1)

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