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Search / Trial NCT00188513

Intensity Modulated Radiation Therapy - Prostate Cancer

Launched by UNIVERSITY HEALTH NETWORK, TORONTO · Sep 12, 2005

Trial Information

Current as of April 28, 2025

Completed

Keywords

ClinConnect Summary

No description provided

Gender

MALE

Eligibility criteria

  • Inclusion Criteria:
  • Histologic diagnosis of adenocarcinoma of the prostate within six months of entry
  • Clinical stage T1B, T1C, T2A-C NX MO (see Appendix 1 for staging). Any Gleason score is eligible for entry, but Gleason score must be determined.
  • Patients with a PSA \>10.0 and Gleason score of 7; or patients with any PSA value and Gleason score of \>8 must have clinically negative lymph nodes as determined by a pelvic CT scan done within 12 weeks of entry. A negative bone scan is required before entry for all patients with Gleason score \>8, or any patient with a Gleason score of 7, and a PSA \>10.
  • The patient must not have received any cytotoxic anticancer therapy. Previous or concurrent hormonal therapy for local disease is acceptable.
  • ECOG performance status of 1 or less
  • Age 80 years old or less
  • Serum PSA \<25 ng/ml within 4 weeks of study entry
  • Informed consent
  • Exclusion Criteria:
  • Patients with history of inflammatory bowel disease or other contraindication to radical radiation therapy
  • Patients with prior colorectal surgery
  • Any prior pelvic radiotherapy. Any prior TURP done \<12 weeks from study entry.
  • Any previous cytotoxic chemotherapy
  • Patients with prior malignancy except non-melanoma skin carcinoma within 5 years of the diagnosis of prostate cancer

About University Health Network, Toronto

University Health Network (UHN), based in Toronto, is a leading academic health sciences center dedicated to advancing patient care through innovative research and education. As a prominent sponsor of clinical trials, UHN integrates cutting-edge scientific discoveries with clinical practice, facilitating the development of new therapies and treatment modalities. With a commitment to improving health outcomes, UHN collaborates with a diverse network of researchers, healthcare professionals, and industry partners, fostering an environment that prioritizes patient safety and ethical standards in clinical research. Through its extensive resources and expertise, UHN plays a pivotal role in transforming healthcare and enhancing the quality of life for patients both locally and globally.

Locations

Toronto, Ontario, Canada

Patients applied

0 patients applied

Trial Officials

Charles Catton, MD

Principal Investigator

Princess Margaret Hospital, Canada

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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