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Prostate Cancer clinical trials

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NCT ID: NCT00538668 Completed - Prostate Cancer Clinical Trials

Radioimmunotherapy in Prostate Cancer Using 177Lu-J591 Antibody

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

The purpose of this study is to test the safety of the experimental drug, 177Lu-J591 and see what effects (good and bad) it has on your prostate cancer. Another purpose is to find the highest dose of the drug that can be given without causing severe side effects.

NCT ID: NCT00537849 Withdrawn - Prostate Cancer Clinical Trials

Investigational Study For the Treatment of Localized (T1c/T2a) Prostate Cancer With High Intensity Focused Ultrasound (HIFU) Using the Sonablate 500 (SB-500) System in Canada

Start date: December 2007
Phase: N/A
Study type: Interventional

An investigational study on the use of HIFU in the management of localized prostate cancer as a primary non-comparative study High intensity focused ultrasound (HIFU) is a non-invasive acoustic ablation technique that uses intersecting, precision focused ultrasound waves to raise the temperature of the target to )80-90 degrees C in 2-3 seconds, destroying the targeted tissues (prostate cancer). The tissue targeting is highly precise, minimizing collateral damage. The overall hypothesis is that HIFU with Sonablate can safely, effectively and selectively ablate prostate cancer tissue, resulting in complete tissue necrosis, in patients diagnosed with localized T1c/T2a prostate cancer, with minimal morbidity. The specific hypothesis is that the Sonablate has the ability to: - COmpletely destroy prostate cancer tissue, without causing damage to the intervening tissue, with a drop in PSA levels to <0.5ng/ml. - Result in negative biopsies for evidence of viable malignant cells after the treatment(12 months if Nadir is not reached or PSA rises from Nadir) - Safely treat localized prostate cancer pts., with minimal and acceptable adverse effects.

NCT ID: NCT00536055 Not yet recruiting - Breast Cancer Clinical Trials

Dyadic Coping in Breast and Prostate Cancer Patients and Their Spouses

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

The purpose of this study is to focus on dyadic coping as one of the main factors that enhance resilience in adjustment to cancer, while also assessing other protective factors for coping with traumatic events. Specifically, the study aims are: 1. To assess the level of post traumatic distress, functional impairment and depression among breast and prostate cancer patients and their spouses. 2. To assess resiliency factors such as flexibility, self efficacy and ego resilience among breast and prostate cancer patients and their spouses. 3. To examine the pattern of dyadic coping at 3 time points: at the beginning and end of radiation therapy, and at six-week follow-up. 4. To examine the relationships between dyadic coping and level of posttraumatic distress and the resilience factors over time (in 3 repeated measures) Different aspects of coping with the trauma of cancer and its treatment may be assessed. Measures of strength and distress amongst patients and their spouses may enable a fuller picture of what types of responses exist, which interventions may be most beneficial, and what other factors may relate to positive coping, increased resilience and quality of life, such as flexibility, and the nature of the couples' dyadic coping.

NCT ID: NCT00535834 Completed - Prostate Cancer Clinical Trials

Studying Stored Samples From Patients With Localized Prostate Cancer Treated on Clinical Trial NCI-00-C-0154

Start date: n/a
Phase: N/A
Study type: Observational

RATIONALE: Studying samples of blood in the laboratory from patients before and after treatment may help doctors learn more about the effects of the treatment on cells. PURPOSE: This clinical trial is studying samples collected from patients with localized prostate cancer who received treatment on clinical trial NCI-00-C-0154.

NCT ID: NCT00534196 Completed - Prostate Cancer Clinical Trials

Implant Radiation Therapy Using Radioactive Iodine in Treating Patients With Localized Prostate Cancer

J-POPS
Start date: July 2005
Phase:
Study type: Observational

RATIONALE: Implant radiation therapy delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. PURPOSE: This clinical trial is studying the side effects and how well implant radiation therapy using radioactive iodine works in treating patients with localized prostate cancer.

NCT ID: NCT00528866 Completed - Prostate Cancer Clinical Trials

Radiation Therapy, Androgen Suppression, and Docetaxel in Treating Patients With High-Risk Prostate Cancer Who Have Undergone Radical Prostatectomy

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

RATIONALE: Specialized radiation therapy that delivers a high-dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. Androgens can cause the growth of prostate cancer cells. Antihormone therapy, such as leuprolide, goserelin, flutamide, or bicalutamide, may lessen the amount of androgens made by the body. 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 radiation therapy together with androgen suppression and docetaxel after surgery may kill any tumor cells that remain after surgery. PURPOSE: This phase II trial is studying how well giving radiation therapy together with androgen suppression and docetaxel works in treating patients with high risk prostate cancer who have undergone radical prostatectomy.

NCT ID: NCT00526591 Terminated - Prostate Cancer Clinical Trials

Everolimus in Treating Patients With Newly Diagnosed Localized Prostate Cancer

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

RATIONALE: Everolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving everolimus before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. PURPOSE: This randomized phase II trial is studying the side effects and how well everolimus works in treating patients with newly diagnosed localized prostate cancer.

NCT ID: NCT00526331 Completed - Prostate Cancer Clinical Trials

Evaluation of Arterial Pressure Based Cardiac Output for Goal-Directed Perioperative Therapy

Start date: August 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the early identification and more precise intervention of operating room (OR) patient fluid administration optimization using arterial pressure-based cardiac output (APCO) yields comparable patient outcome as fluid administration optimization using a global standard care method.

NCT ID: NCT00525720 Active, not recruiting - Prostate Cancer Clinical Trials

Brachytherapy for Prostatic Carcinoma Patients

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

The goal of this clinical research study is to learn if a prostate implant (brachytherapy) can help to control intermediate risk prostate cancer. The safety of this procedure will also be studied. Prostate brachytherapy is performed by inserting permanent seeds (which are radioactive pellets) into your prostate in order to treat the prostate cancer with radiation therapy.

NCT ID: NCT00524823 Recruiting - Prostate Cancer Clinical Trials

Early Detection of Prostate Cancer by FACS

FACS
Start date: August 2007
Phase: Phase 4
Study type: Observational

Early detection of prostrate cancer and development of metastases. The research will attempt to match the SCM test (structuredness of the cytoplasmic matrix) in lymphocytes as an early cancer detection test using Florescent Activated Cell Sorting (FACS) as a replacement for the CellScan instrument. The test is based on measurement of cellular changes in response to the specific prostate antigen, PSA.