Expired Study
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Madison, Wisconsin 53792


Purpose:

The purpose of this study is to examine the clinical feasibility and efficacy of uing IMRT to escalate the biologically effective dose to the pelvic lymph nodes in a short course of radiation therapy. An increased total and biologically effective dose will be delivered to the pelvic lymph nodes (56 Gy at 2 Gy/fraction). The prostate will receive standard "short course" IMRT of radiation (70 Gy at 2.5 Gy/fraction).


Criteria:

Inclusion Criteria: - Prostate cancer stage T-T3 - Predicted risk of lymph node involvement > 15% - Gleason > 7 Exclusion Criteria: - Distance metastases - Use of anti-coagulant therapy


NCT ID:

NCT00214136


Primary Contact:

Principal Investigator
Mark Ritter, MD, PhD
University of Wisconsin, Madison


Backup Contact:

N/A


Location Contact:

Madison, Wisconsin 53792
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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