Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 4:14 PM
Ignite Modification Date:
2025-12-24 @ 4:14 PM
NCT ID:
NCT00001266
Eligibility Criteria:
INCLUSION CRITERIA:
Patients must have a histologic diagnosis of carcinoma of the prostate and must not have had a trial of hormonal therapy or chemotherapy.
Patients must be 18 years of age and an SGOT/SGPT within 2 times of normal.
Patients must have stage D2 prostate carcinoma or State D1 disease with a Gleason grade 7 or above (poorly differentiated).
No other malignancy except curatively treated basal cell cancer of the skin.
Performance status ECOG of 0-3.
Ability to give informed consent.
No history of bleeding diathesis. Patients with a history of peptic ulcer disease will be eligible if the ulcer is shown to be resolved by a barium study.
No history of cerebrovascular event, either thrombotic or hemorrhagic.
No current clinical signs of congestive heart failure, angina pectoris or myocardial infarction. Patient cannot be on calcium channel blockers such as Nifedipine, Diltiazem, or Verapamil.
No clinical or radiographic evidence of brain metastases.
Patients with extensive liver replacement (greater than 50%) by tumor will be ineligible.
Patients must have a creatinine lest than or equal 2.5 mg/dl or creatinine clearance of greater than or equal to 40 ml/min.
Patients must have adequate hepatic function (bilirubin less than 1.5mg%).
If the patient has white cells in his urinalysis or other evidence of a urinary tract infection, this must be evaluated and appropriate therapy initiation prior to the initiation of therapy.
Patients must not have received chemotherapy.
An absolute granulocyte count greater than 1,500; platelet count greater than 100,000; Fibrinogen greater than 200 mg/dl; Hgb greater than or equal to 9 gm/dl.
Reliability of the patient to take oral medication, go home and return for follow-up and treatment.
Healthy Volunteers:
False
Sex:
MALE
Study:
NCT00001266
Study Brief:
Protocol Section:
NCT00001266