Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention

Outcome Measure:

change in blood PSA levels

Outcome Time Frame:

6 months

Safety Issue:

No

Principal Investigator

Jay H Fowke, PhD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Vanderbilt University

Authority:

United States: Institutional Review Board

Study ID:

041001

NCT ID:

NCT00579332

Start Date:

January 2005

Completion Date:

December 2006

Related Keywords:

• Biochemical Failure
• PSA
• biochemical failure

Name	Location
Vanderbilt_University	Nashville, Tennessee  23233