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Prostatic Neoplasms clinical trials

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NCT ID: NCT00446901 Completed - Prostate Cancer Clinical Trials

Selenium and Prostate Cancer: Clinical Trial on Availability to Prostate Tissue and Effects on Gene Expression

SePros
Start date: June 2007
Phase: N/A
Study type: Interventional

The aim of this study is to determine whether selenium supplementation leads to changes in selenium levels and gene expression profiles in prostate tissue.

NCT ID: NCT00446836 Completed - Prostatic Neoplasms Clinical Trials

Efficacy and Safety Study of Xyotax to Treat Prostate Cancer

Start date: March 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Xyotax, a conjugate of the taxane drug paclitaxel, is effective in the treatment of prostate cancer that is no longer responsive to hormone therapy.

NCT ID: NCT00444730 Completed - Prostate Cancer Clinical Trials

Urology Database for Outcomes Research

Start date: January 2007
Phase: N/A
Study type: Observational

The purpose of initiating the urology database is to collect relevant retrospective data via chart review related to patients undergoing radical prostatectomy via the retropubic, perineal, laparoscopic, and robotic assisted laparoscopic approaches and InterStim implantation. This data will be utilized to evaluate the health benefits and outcomes of each of these procedures to enhance care and treatment.

NCT ID: NCT00442000 Completed - Prostate Cancer Clinical Trials

Outcomes Comparison of Robotic, Retropubic, and Perineal Prostatectomy

Start date: January 2005
Phase: N/A
Study type: Observational

Compare peri-operative and postoperative outcomes of the three different surgical approaches to prostatectomy

NCT ID: NCT00441337 Completed - Prostate Cancer Clinical Trials

A Study of MDX-1106 in Patients With Selected Refractory or Relapsed Malignancies

MDX1106-01
Start date: August 2006
Phase: Phase 1
Study type: Interventional

To evaluate the safety, tolerability, efficacy, and pharmacokinetics of MDX-1106 when administered to patients with advanced non-small cell lung cancer, colorectal cancer, malignant melanoma, clear cell renal cell cancer or hormone refractory prostate cancer

NCT ID: NCT00439751 Completed - Prostate Cancer Clinical Trials

Immediate Versus Deferred Androgen Deprivation Therapy,Goserelin for Recurrent Prostate Cancer After Radical Radiotherapy

ELAAT
Start date: April 2007
Phase: Phase 3
Study type: Interventional

This is a prospective, multicentre, open-labelled, randomized controlled trial comparing the efficacy of immediate versus deferred androgen deprivation therapy (ADT) using goserelin (Zoladex®) in men with recurrent prostate cancer after radical radiotherapy. 1100 patients will be accrued from participating Canadian Urological Oncology Group sites in an estimated time of 3 years. First analysis is planned for 7 years after study recruitment is completed.

NCT ID: NCT00439270 Completed - Clinical trials for Metastatic Prostate Cancer

Study of Dasatinib and Docetaxel in Metastatic Hormone Refractory Prostate Cancer

Start date: July 2007
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to find the recommended doses of dasatinib and docetaxel given in combination to men with metastatic hormone refractory prostate cancer and to assess the pharmacokinetic interactions between the 2 drugs.

NCT ID: NCT00438464 Completed - Clinical trials for Adenocarcinoma of the Prostate

Finasteride in Treating Patients With Stage II Prostate Cancer Who Are Undergoing Surgery

Start date: February 2007
Phase: Phase 2
Study type: Interventional

This randomized phase II trial studies how well finasteride works in treating patients with stage II prostate cancer who are undergoing surgery. Testosterone can cause the growth of prostate cancer cells. Hormone therapy using finasteride may fight prostate cancer by lowering the amount of testosterone the body makes. Giving finasteride before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed.

NCT ID: NCT00436956 Completed - Prostate Cancer Clinical Trials

AZD2171 to Treat Prostate Cancer

Start date: October 16, 2006
Phase: Phase 2
Study type: Interventional

Background: - AZD2171 (Cediranib) is an experimental drug that inhibits formation of new blood vessels. - Tumors need new blood vessels to grow. Preventing the growth of new blood vessels with AZD2171 may inhibit tumor growth. Objectives: -To determine the effectiveness and side effects of AZD2171 in patients with prostate cancer that has metastasized (spread beyond the primary site). Eligibility: - Males 18 years of age and older with androgen-independent prostate cancer that has metastasized. - Patients must have received prior treatment with docetaxel. Design: Patients take one AZD2171 by mouth every day in 28-day treatment cycles and undergo the following procedures: - 1- to 2-day hospitalization at the start of the study for biopsies and blood measurements to determine the level of AZD2171 in the bloodstream. Blood is drawn immediately before the first dose, and 0.25 hr, 0.5 hr, 1 hr, 2 hr, 4 hr, 6 hr, 8 hr, 12 hr, 24 hr, and 48 hours after the dose is taken. - Blood tests before starting treatment and then monthly to determine the level of vascular endothelial growth factor receptor ( VEGFR), a protein involved in blood vessel formation. - Magnetic resonance imaging (MRI) scans once a month to evaluate blood flow. - Tumor biopsies (optional) both before and after the second and sixth treatment cycles. - Clinic visits every 4 weeks, including various routine and research blood tests, urine test and electrocardiogram. - Computed tomography (CT) scan of the chest, abdomen, and pelvis every 8 weeks - Bone scan every 8 weeks Patients record all doses of AZD2171 taken or missed in a pill diary. They record their blood pressure at least once daily in a blood pressure diary. Treatment may continue as long as the patient tolerates the AZD2171 and the cancer does not worsen.

NCT ID: NCT00436839 Completed - Prostatic Neoplasms Clinical Trials

Taxotere Prostate Cancer New Indication Registration Trial in China

Start date: January 2007
Phase: Phase 3
Study type: Interventional

To compare overall survival after receiving mitoxantrone and prednisone or docetaxel and prednisone in subjects with hormone-refractory metastatic prostate cancer.