Westmont, Illinois 60559


Purpose:

This study will investigate health related quality of life factors in patients undergoing low dose rate prostate brachytherapy. Patients will be randomized to Iodine-125 Thinstrand (for use with 20 g needles) or Rapidstrand (for use with standard 18 g needles). Urinary, bowel, sexual function and bother will be measured by the EPIC questionnaire at various time intervals.


Criteria:

Inclusion Criteria: - Histologically confirmed adenocarcinoma of the prostate, clinical stage T1c - T2b, N0, M0 - Greater than or equal to 40 years of age - Low and Low- Intermediate Risk prostate cancer - Prostate volumes by TRUS ≤ 60 cc - I-PSS score < 25 (alpha blockers allowed) - Signed study-specific informed consent form prior to study entry Exclusion Criteria: - Lymph node involvement (N1) - Evidence of distant metastases (M1) - Radical surgery for carcinoma of the prostate - Prior pelvic radiation - Major medical or psychiatric illness, which in the investigator's opinion would prevent completion of treatment and would interfere with follow- up or ability to complete questionnaires - Hip prosthesis - Inability or refusal to provide informed consent - Evidence of Previous TURP - Prior hormone therapy - Prior TURP


NCT ID:

NCT01379742


Primary Contact:

Principal Investigator
Brian J Moran, MD
Chicago Prostate Center


Backup Contact:

N/A


Location Contact:

Westmont, Illinois 60559
United States

Brian J Moran, MD
Phone: 630-654-2515
Email: seeds@prostateimplant.com

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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