Prostate Cancer Clinical Trial

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Hypofractionated Proton Radiation Therapy for Low and Intermediate Risk Prostate Cancer

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Summary

The purpose of this trial is to give a shorter course (5 ½-6 weeks) of proton radiation that has as little side effects on normal bladder and rectal tissues as the usual longer course (8 weeks) of proton radiation, without decreasing the chance of killing prostate cancer cells.

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Eligibility Criteria

Inclusion Criteria:

Prostate cancer.
Gleason score 2-6 or 7.
PSA ≤ 20 ng/ml.

Exclusion Criteria:

Previous prostate cancer surgery or pelvic radiation.
Prior/concurrent systemic chemotherapy for prostate cancer.
Active inflammatory bowel disease (Crohn's disease, diverticulitis or ulcerative colitis) affecting the rectum.
History of hip replacement.
Prior intrapelvic surgery.
Taking Saw Palmetto or methotrexate and unable or unwilling to discontinue its uses during radiation.
Receiving continuous and current anticoagulation with Warfarin sodium (Coumadin), Clopidogrel bisulfate (Plavix), dabigatran etexilate mesylate (Pradaxa),enoxaparin sodium (Lovenox), or aspirin/er dipyridamole (Aggrenox).

Study is for people with:

Prostate Cancer

Estimated Enrollment:

361

Study ID:

NCT01368055

Recruitment Status:

Active, not recruiting

Sponsor:

University of Florida

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There is 1 Location for this study

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University of Florida Proton Therapy Institute
Jacksonville Florida, 32209, United States

How clear is this clinincal trial information?

Study is for people with:

Prostate Cancer

Estimated Enrollment:

361

Study ID:

NCT01368055

Recruitment Status:

Active, not recruiting

Sponsor:


University of Florida

How clear is this clinincal trial information?

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