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Prostate Cancer clinical trials

View clinical trials related to Prostate Cancer.

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NCT ID: NCT00670527 Recruiting - Prostate Cancer Clinical Trials

[18F] Fluorocholine FCH Positron Emission Tomography (PET)/Computed Tomography (CT) for Detection of Prostate Cancer Lymph Nodes Metastases

PROPET
Start date: January 2008
Phase: N/A
Study type: Interventional

The objective of this trial is to assess the value of 18F-choline PET/CT for the detection of regional lymph node metastases from prostate cancer. In addition, the investigators want to evaluate whether 18F-choline PET/CT can replace lymphadenectomy for the staging of prostate cancer.

NCT ID: NCT00670046 Terminated - Prostate Cancer Clinical Trials

Valproic Acid in Treating Patients With Progressive, Non-Metastatic Prostate Cancer

Start date: May 2008
Phase: Phase 2
Study type: Interventional

RATIONALE: Valproic acid may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It is not yet known whether valproic acid is more effective than observation in treating patients with prostate cancer. PURPOSE: This randomized phase II trial is studying how well valproic acid works in treating patients with progressive, non-metastatic prostate cancer.

NCT ID: NCT00669656 Completed - Prostate Cancer Clinical Trials

Herbal Therapy for Treatment of Recurrent Prostate Cancer

Start date: July 6, 2008
Phase: Phase 2
Study type: Interventional

This study is about Prostate Health Cocktail, a combination supplement that contains vitamin D3, vitamin E, selenium, green tea extract, saw palmetto, lycopene, and soy derivatives. This product is currently available on the market, as herb and vitamin supplements are not regulated by the FDA. Each ingredient has been studied in prostate cancer cells and/or in patients with prostate cancer. At the doses included in this supplement, no serious side effects have been reported. The purpose of this study is to find out whether Prostate Health Cocktail can lower your PSA. Additionally, we will be looking to see whether taking this treatment causes any unexpected side effects, and whether certain blood tests can inform us about your disease status in addition to your PSA

NCT ID: NCT00669162 Completed - Prostate Cancer Clinical Trials

Postoperative Radiation Therapy, Hormonal Therapy and Concurrent Docetaxel for High Risk Pathologic Prostate Cancer

Start date: August 2012
Phase: Phase 1/Phase 2
Study type: Interventional

Following a radical prostatectomy and lymph node sampling, eligible patients will undergo post-operative radiation therapy, concurrent weekly docetaxel chemotherapy , and hormonal therapy (Casodex daily and Zoladex every 3 months for 2 times or Lupron 22.5 mg im every 3 months for 2 times).

NCT ID: NCT00668642 Completed - Prostate Cancer Clinical Trials

Effect of Dutasteride on Androgen-Response Gene Expression in Patients With Advanced Prostate Cancer

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

The purpose of this study is to determine if the drug dutasteride increases expression of genes that slow the growth of prostate cancer during treatment with intermittent androgen ablation therapy (hormone therapy).

NCT ID: NCT00668083 Completed - Prostate Cancer Clinical Trials

Observational Retrospective Trial on Sequential Hormonal Therapy in Patients With Prostate Cancer

Sorse
Start date: September 2007
Phase: N/A
Study type: Observational

Observational Retrospective trial on sequential hormonal therapy in patients with Prostate Cancer

NCT ID: NCT00667888 Active, not recruiting - Prostate Cancer Clinical Trials

A Phase III Intensity Radiotherapy Dose Escalation for Prostate Cancer Using Hypofractionation

Start date: January 3, 2001
Phase: Phase 3
Study type: Interventional

The goal of this clinical research study is to compare using external beam radiotherapy with intensity modulated beams for fewer days at a higher dose per day to the same type of therapy for more days at a lower dose per day in the treatment of prostate cancer. The safety of these treatments will also be studied and compared.

NCT ID: NCT00667862 Completed - Prostate Cancer Clinical Trials

Efficacy and Safety Study of Panobinostat in Participants With Metastatic Hormone Refractory Prostate Cancer

Start date: March 18, 2008
Phase: Phase 2
Study type: Interventional

This Phase II single dose study was designed to characterize the safety, tolerability, and efficacy of intravenous (i.v.) panobinostat as a single-agent treatment in participants with hormone refractory prostate cancer.

NCT ID: NCT00667641 Completed - Breast Cancer Clinical Trials

Paclitaxel and Bortezomib in Treating Patients With Metastatic or Unresectable Malignant Solid Tumors

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

RATIONALE: Drugs used in chemotherapy, such as paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Bortezomib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving paclitaxel together with bortezomib may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of paclitaxel and bortezomib in treating patients with metastatic or unresectable malignant solid tumors.

NCT ID: NCT00667069 Active, not recruiting - Prostate Cancer Clinical Trials

Triptorelin and Radiation Therapy in Treating Patients Who Have Undergone Surgery for Intermediate-Risk Stage III or Stage IV Prostate Cancer

Start date: April 7, 2008
Phase: Phase 3
Study type: Interventional

RATIONALE: Androgens can cause the growth of prostate cancer cells. Antihormone therapy, such as triptorelin, may lessen the amount of androgens made by the body. Radiation therapy uses high-energy x-rays to kill tumor cells. It is not yet known whether giving triptorelin and radiation therapy soon after surgery or later after surgery is more effective in treating prostate cancer. PURPOSE: This randomized phase III trial is studying giving triptorelin and radiation therapy soon after surgery to see how well it works compared with giving them later after surgery in treating patients who have undergone surgery for intermediate-risk stage III or stage IV prostate cancer.