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Prostate Cancer clinical trials

View clinical trials related to Prostate Cancer.

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NCT ID: NCT00450229 Completed - Prostate Cancer Clinical Trials

Diindolylmethane in Treating Patients Undergoing Surgery for Stage I or Stage II Prostate Cancer

Start date: February 2007
Phase: Phase 1
Study type: Interventional

Giving diindolylmethane, a substance found in cruciferous vegetables, may help doctors learn more about how diindolylmethane is used by the body. This randomized phase I trial is studying the side effects and best dose of diindolylmethane compared with a placebo in treating patients undergoing radical prostatectomy for stage I or stage II prostate cancer.

NCT ID: NCT00448695 Completed - Prostate Cancer Clinical Trials

MRI Targeted Focal Laser Thermal Therapy of Biopsy Confirmed Prostate Cancer

Start date: March 2007
Phase: Phase 1
Study type: Interventional

The objective of this study is to establish the safety of MRI targeted laser thermal treatment for men with biopsy confirmed early stage low grade single sector prostate cancer.

NCT ID: NCT00447616 Terminated - Prostate Cancer Clinical Trials

Prostatectomy Prospective Database

Start date: October 2003
Phase: N/A
Study type: Observational

The purpose of establishing the database is to evaluate the effects of surgical removal of the prostate (prostatectomy) and cryosurgery on prostate cancer, quality of life, and overall health.

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: 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: NCT00444639 Terminated - Prostate Cancer Clinical Trials

Study to Assess the Non-inferiority of Pamorelin® 11,25mg SC Injected Versus Pamorelin® 11,25mg IM Injected in Patients Suffering From Advanced Prostate Cancer (PAMOJECT)

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

The active ingredient of Pamorelin® 11,25 mg is Triptorelin. Triptorelin is a substitute for a natural hormone produced in the body called Gonadotrophin-releasing hormone (GnRH). GnRH is a hormone secreted by hypothalamus (a gland located in brain) and controls the production of sex hormones (eg testosterone in men) in other organs in the body. The growth of prostate cancer cells, one of the most common cancers in men, is induced by the hormone testosterone. Hormonotherapy is one of treatments available to treat this type of disease by controlling the testosterone serum level. Pamorelin® 11,25 mg is normally injected in the muscle but this type of injection is not suitable for every patient. Therefore the primary purpose of this study is to assess the non-inferiority of the 12-week triptorelin formulation Pamorelin® 11,25 mg administered via subcutaneous (SC) injection as compared to Pamorelin® 11,25 mg administered via standard intramuscular (IM) injection based on the percentage of patients presenting a testosterone level ≤ 50 ng/dl at week 24.

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: NCT00441532 Completed - Prostate Cancer Clinical Trials

Study On Lidocaine Vs. Placebo Pain Control During Transrectal Ultrasound Guided Prostate Biopsy

Start date: August 2005
Phase: N/A
Study type: Interventional

Patients at risk for having prostate cancer usually undergo a biopsy of their prostate. This is most often done in the private urology office. Recent studies have suggested that injection of local anesthesia (lidocaine) near the nerves of the prostate will improve pain sensation during the biopsy procedure. Local anesthesia can be given through a separate needle through the rectal probe just prior to biopsy. However, many urologists to date perform their biopsies without anesthesia. Some claim that the needle used for anesthesia causes pain itself. Others claim that the pain is so minimal that the additional use of lidocaine (and extra time) is not necessary. We plan to reexamine the use of lidocaine and perform the first study where each patient will receive lidocaine and placebo on separate sides of their prostate.

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.