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Prostatic Neoplasms clinical trials

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NCT ID: NCT00589966 Completed - Prostate Cancer Clinical Trials

Coping in African American Prostate Cancer Survivors

CAAPS
Start date: May 2007
Phase: N/A
Study type: Interventional

This study will test the effectiveness of an 8-week group intervention for African American men who have been treated for prostate cancer. The group intervention is based on 1) the cognitive-behavioral theoretical approach to improving adjustment to cancer and 2) masculinity theory as it relates to coping strengths and preferences in men. We will test the effectiveness of this coping skills intervention for improving survivors' quality of life in 4 areas: 1) distress related to sexual, urinary, and bowel symptoms; 2) self-confidence for managing symptoms; 3) overall emotional functioning; and 4) overall physical functioning. The effect of the coping skills group intervention in these 4 areas will be compared to a comparison intervention in which African American men will receive basic education about prostate cancer, but will not participate in coping skills training.

NCT ID: NCT00589472 Completed - Clinical trials for Prostate Adenocarcinoma

Androgen Deprivation Therapy and Vorinostat Followed by Radical Prostatectomy in Treating Patients With Localized Prostate Cancer

TARGET
Start date: November 2007
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well androgen deprivation therapy and vorinostat followed by radical prostatectomy works in treating patients with prostate cancer that has not spread to other parts of the body. Androgens can cause the growth of prostate cancer cells. Antihormone therapy, such as bicalutamide, goserelin acetate, and leuprolide acetate, may lessen the amount of androgens made by the body. Vorinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving androgen deprivation therapy and vorinostat before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed.

NCT ID: NCT00589420 Completed - Prostate Cancer Clinical Trials

Sorafenib and Docetaxel in Patients With Prostate Cancer That Did Not Respond to Previous Hormone Therapy

Start date: July 27, 2007
Phase: Phase 2
Study type: Interventional

RATIONALE: Sorafenib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving sorafenib together with docetaxel may kill more tumor cells. PURPOSE: This phase II trial is studying giving sorafenib together with docetaxel to see how well it works in treating patients with metastatic androgen-independent prostate cancer.

NCT ID: NCT00588679 Completed - Prostate Cancer Clinical Trials

Magnetic Resonance Spectroscopic Imaging of the Prostate at 3 Tesla

Start date: August 22, 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the benefits of Magnetic Resonance Imaging (MRI) combined with Magnetic Resonance Spectroscopic Imaging (MRSI), on an instrument called a 3.0 Tesla (T) MR scanner.

NCT ID: NCT00587964 Completed - Breast Cancer Clinical Trials

Phase II Trial of Stereotactic Radiosurgery Boost Following Surgical Resection for Brain Metastases

Start date: June 2004
Phase: Phase 2
Study type: Interventional

For patients who have one or two metastases in the brain, the tumor(s) can often be removed with surgery to relieve symptoms from the tumor(s) and to improve survival. However, about half of all patients who have the tumor(s) removed with surgery will develop regrowth (recurrence) of the tumor. To prevent this regrowth of tumor, some patients receive radiation to the entire brain (whole brain radiation) after surgery. This involves daily treatment for about two to three weeks, and may cause long-term neurological problems, such as memory loss. Stereotactic radiosurgery (SRS) is sometimes used instead of surgery to treat brain metastasis. This involves the use of a special head frame and sophisticated computer programs that enable us to deliver a high dose of radiation to a small focused area of the brain in only one treatment. Research has shown that the results of treatment with SRS are as good as surgical removal of the tumor. SRS and surgical resection are considered the standard options for the treatment of brain metastases. This Phase II clinical trial is studying the combination of these two techniques. The purpose of this study is to evaluate the use of SRS following surgical removal of brain metastases. The outcomes we will be looking at are tumor regrowth after treatment and side effects of treatment.

NCT ID: NCT00587431 Completed - Prostate Cancer Clinical Trials

Docetaxel With Rapid Hormonal Cycling as a Treatment for Patients With Prostate Cancer

Start date: July 2003
Phase: Phase 2
Study type: Interventional

We postulate that multiple apoptototic events are indusce through testosterone depletion and repletion with taxotere given in conjunction with androgen withdrawal.

NCT ID: NCT00585962 Completed - Prostate Cancer Clinical Trials

Proton Beam Radiation Therapy for Early Stage Adenocarcinoma of the Prostate

Start date: February 2004
Phase: Phase 2
Study type: Interventional

The primary purpose of this study is to determine if high doses of radiation using proton beam can be given safely with low and acceptable side effects. This study will also gather data to determine the ability of the proton beam to eradicate prostate cancer. Proton beam radiation is a very accurate kind of treatment that has been shown to affect less normal tissue than a regular radiation beam.

NCT ID: NCT00584792 Completed - Prostate Cancer Clinical Trials

Diet, Genetic Variation and Prostate Cancer Among African Americans

Start date: August 2006
Phase: N/A
Study type: Observational

This is a single center pilot study to asses the feasibility of conducting a larger population-based study. It is an investigator-initiated study funded yb the UC Davis Cancer Center's Development Award Program. The hypothesis is that the percent african ancestry in an individual may determine their prognosis if diagnosed with prostate cancer.

NCT ID: NCT00584532 Completed - Prostate Cancer Clinical Trials

Effects of a Genistein Concentrated Polysaccharide (GCP) for Prostate Cancer on Active Surveillance.

GCP
Start date: November 2003
Phase: Phase 2/Phase 3
Study type: Interventional

Genistein Combined Polysaccharide (GCP) may play a role as a secondary chemopreventive agent in the treatment of localized prostate cancer.

NCT ID: NCT00583752 Completed - Clinical trials for Recurrent Prostate Cancer

Phase II Study of Adenovirus/PSA Vaccine in Men With Recurrent Prostate Cancer After Local Therapy APP21

APP21
Start date: December 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether vaccination with the Ad/PSA vaccine will induce an anti-PSA immunity that will result in the destruction of the remaining prostate cancer cells.