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Prostate Cancer clinical trials

View clinical trials related to Prostate Cancer.

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NCT ID: NCT00918229 Completed - Prostate Cancer Clinical Trials

Pilot Study to Assess the Safety and Efficacy of BioProtect Balloon in Prostate Cancer Subjects

Start date: June 2009
Phase: N/A
Study type: Interventional

Primary Goal The study's primary goal is to assess the safety of the BioProtect biodegradable balloon implant and implantation procedure, in prostate cancer subjects undergoing routine radiation therapy (XRT) treatment. Safety of the BioProtect device will be assessed by reporting adverse events. Secondary Goal The study's secondary goal is to evaluate the effectiveness of the BioProtect biodegradable balloon implant in prostate cancer subjects undergoing routine XRT treatment. Effectiveness will be assessed in terms of increased distance between anterior rectal wall and prostate and noticeable reduction of isodose to the rectum.

NCT ID: NCT00916123 Completed - Prostate Cancer Clinical Trials

Docetaxel/Prednisone Plus Fractionated 177Lu- J591 Antibody for Metastatic, Castrate-resistant Prostate Cancer

Start date: May 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to test the effectiveness of the experimental drug, 177Lu-J591 antibody in combination with docetaxel chemotherapy against metastatic, castrate-resistant prostate cancer.

NCT ID: NCT00915031 Completed - Prostate Cancer Clinical Trials

Use of Hypothermia During Robotic Prostatectomy

Start date: August 2009
Phase: N/A
Study type: Interventional

Robotic assisted laparoscopic radical prostatectomy (RLP) has gained widespread acceptance as a standard treatment for clinically localized prostate cancer. Despite the enhanced visualization and precise dissection afforded by the robotic platform, two major comorbidities affect a significant number of men: incontinence and erectile function. Urinary continence and erectile function It is commonly believed that the most important factor affecting continence is preservation of the external urinary sphincter complex which lies just below the prostate. Trauma to the urethral tissue itself after it is transected from the prostate and damage to the autonomic nerves that control this sphincter may lead to sphincteric dysfunction. In addition, dissection of the bladder may lead to bladder irritability which also plays a role in incontinence. Surgical removal of the prostate also causes significant inflammatory damage to the pelvic floor which likely delays recovery of urinary continence. The same trauma issues apply to sexual function. One possible method to protect the nerves and other tissues from operative trauma may be the use of local hypothermia (cold-ischemia) to the pelvis. Local tissue hypothermia using ice, ice slush, or cold irrigation has been safely and routinely used for decades in humans during brain, heart, and kidney surgery to minimize organ damage. Yet, this technique has never been applied to prostate surgery. We will accomplish local cooling of the pelvis using a cooling balloon inserted into the rectum. The cooling balloon is powered by an FDA approved cooling system developed by Innercool therapies. Temperatures of 57-86 degrees F (22+/-8 degrees C).

NCT ID: NCT00913263 Completed - Prostate Cancer Clinical Trials

An Efficacy and Safety Study With Licroca Depot, a Controlled Release Product, Injected Into the Prostate

2-HOF
Start date: June 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The primary objective was to evaluate efficacy of a single dose of Liproca Depot in patients with localized prostate cancer. Primary efficacy variable was the proportion of patients showing PSA nadir. 24 Caucasian men, with a mean age at inclusion of 68.4 years, with localized prostate cancer were injected once with a ready made paste including 600 mg 2-hydroxyflutamide (Liproca Depot) into the site of the prostate where the tumour was localized. The patient was monitored for prostate-specific antigen (PSA) for maximum 6 months or to progression within this time period. The primary endpoint showed interesting results with high success rate (83%), i.e. proportion of patients (Responders) that reached plasma PSA nadir.

NCT ID: NCT00913068 Completed - Prostate Cancer Clinical Trials

Postoperative Pain Control for Prostatectomy

TAP
Start date: July 2009
Phase: N/A
Study type: Interventional

The researchers propose to investigate a relatively new anesthetic procedure, in order to maximize patient comfort and minimize the use of narcotics after a radical prostatectomy.

NCT ID: NCT00908674 Completed - Prostate Cancer Clinical Trials

Androcur Effects on Quality of Life

Start date: June 2008
Phase: N/A
Study type: Observational

Androcur is an antiandrogenic drug, which blocks the action of male sex hormones. Androcur is used for treatment of advanced prostate cancer. This study investigates the effect of Androcur on quality of life of prostate cancer patients who are taking the drug for 12 months

NCT ID: NCT00908141 Completed - Prostate Cancer Clinical Trials

GM-CSF in Treating Patients With Relapsed Prostate Cancer

Start date: June 2006
Phase: Phase 2
Study type: Interventional

RATIONALE: Colony stimulating factors, such as GM CSF, may increase the number of immune cells found in bone marrow or peripheral blood. It is not yet known which GM-CSF regimen is more effective in treating patients with prostate cancer. PURPOSE: This randomized phase II trial is studying how well GM-CSF works in treating patients with relapsed prostate cancer.

NCT ID: NCT00905086 Completed - Breast Cancer Clinical Trials

Psychosocial Adjustment After Radiation Therapy in Patients With Cancer

Start date: August 2008
Phase: N/A
Study type: Observational

RATIONALE: Gathering information about psychological and social adjustment after radiation therapy in patients with cancer may help doctors plan the best treatment. PURPOSE: This clinical trial is studying psychosocial adjustment after radiation therapy in patients with breast cancer, colorectal cancer, lung cancer, or prostate cancer.

NCT ID: NCT00901342 Completed - Prostate Cancer Clinical Trials

Open Label Study of Sipuleucel-T

Start date: August 2009
Phase: Phase 2
Study type: Interventional

This is a Multicenter, Open Label, Phase 2 Study of Sipuleucel-T in Men with Metastatic Castrate Resistant Prostate Cancer (CRPC).

NCT ID: NCT00900835 Completed - Breast Cancer Clinical Trials

Pain and Fatigue Management in Patients With Breast Cancer, Prostate Cancer, Colon Cancer, or Lung Cancer

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

RATIONALE: Collecting information over time about patients' and health care providers' understanding of pain and fatigue and providing education about pain and fatigue management may improve quality of life. PURPOSE: This clinical trial is studying pain and fatigue management in patients with breast cancer, prostate cancer, colon cancer, or lung cancer.