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Prostatic Neoplasms clinical trials

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NCT ID: NCT01144897 Completed - Prostate Cancer Clinical Trials

PET Acetate for Castrate-Resistant Prostate Cancer on Chemotherapy

Start date: May 2010
Phase: Phase 1
Study type: Interventional

One purpose of this research study is to examine if a special type of imaging test, a positron emission tomography (PET) scan using the radioactive material [C-11] acetate, will be helpful in detecting prostate cancer lesions in subjects with castrate-resistant prostate cancer (CRPC). This PET scan will be combined with a computed tomography (CT) scan taken during the same imaging session. The other purpose of the PET-CT scan using [C-11] acetate (PET Acetate Scan) is to assist in identifying who is responding to the treatment (docetaxel chemotherapy).

NCT ID: NCT01138527 Completed - Prostate Cancer Clinical Trials

Prostate Cancer Localization With a Multiparametric Magnetic Resonance (MR) Approach

PCa-MAP
Start date: June 2010
Phase:
Study type: Observational

The primary objective of this prospective multi-centre study is to prove the diagnostic accuracy of in vivo 3T multi-modality Magnetic Resonance Imaging (high resolution T2-weighted MRI, DCE-MRI, MRSI and DWI techniques) in distinguishing carcinoma from other prostate tissue. The gold standard for distinguishing the tissue types is the analysis of whole-mount sections of the resected prostate by a genitourinary histopathologist.

NCT ID: NCT01136226 Completed - Prostate Cancer Clinical Trials

Evaluate Recovery of Testosterone for Patients Using Eligard

Eligard
Start date: October 2003
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if testosterone will recover to 90% by year 1 after using Eligard.

NCT ID: NCT01133704 Completed - Clinical trials for Hormone-Refractory Prostate Cancer

Immunotherapy With APC8015 (Sipuleucel-T, Provenge) for Asymptomatic, Metastatic, Hormone-Refractory Prostate Cancer

Start date: May 2000
Phase: Phase 3
Study type: Interventional

This is a randomized, double blind, placebo controlled trial of immunotherapy with autologous antigen-loaded dendritic cells (Provenge, APC8015) for asymptomatic, metastatic, hormone-refractory prostate cancer.

NCT ID: NCT01123434 Completed - Clinical trials for 2 Years PSA Recurrence Rate

Immediate Postoperative Adjuvant Hormonal Treatment in High Risk Localised or Locally Advanced Prostate Cancer Patients.

Start date: April 2010
Phase: N/A
Study type: Observational

The primary objective is to assess the efficacy of immediate postoperative adjuvant hormonal treatment according to 2 year PSA recurrence rate in high risk localised or locally advanced Chinese prostate cancer patients.The secondary objective is to assess the quality of life(QoL)of the high risk localised or locally advanced Chinese prostate cancer patients with immediate postoperative adjuvant hormonal treatment and get the information of immediate postoperative adjuvant hormonal treatment (including the regimen, dosage and duration).

NCT ID: NCT01122121 Completed - Clinical trials for Prostatic Neoplasms, Locally Advanced

Leuprorelin Associated With Radiotherapy Versus Leuprorelin Alone in T3 - T4 or pT3 (on Biopsy) N0, M0 Prostate Cancer

Start date: March 2000
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the efficacy and safety of combined radiotherapy and hormone therapy and hormone therapy alone in the treatment of clinically locally advanced prostate cancer (T3-T4 or pT3 on biopsy, N0, M0).

NCT ID: NCT01120470 Completed - Clinical trials for Castration Resistant Prostate Cancer

OGX-427 in Castration Resistant Prostate Cancer Patients

Start date: September 2010
Phase: Phase 2
Study type: Interventional

This study is being offered to patients who have castrate-resistant (also known as hormone-refractory) prostate cancer. The cancer has metastasized or spread outside the prostate area to other parts of the body or has recurred in the pelvic area after treatment. The purpose of this clinical research study is to determine whether OGX-427 is able to slow the progression of prostate cancer and symptoms of disease when given with prednisone better than when prednisone is given alone in patients with prostate cancer whose disease has spread outside the prostate area. Research Hypothesis: That adding OGX-427 to prednisone treatment will produce a progression free rate of 20%.

NCT ID: NCT01120262 Completed - Prostate Cancer Clinical Trials

S9346A Blood Samples From Patients With Metastatic Prostate Cancer Previously Treated With Bicalutamide and Goserelin

Start date: February 2010
Phase: N/A
Study type: Observational

RATIONALE: Studying samples of blood in the laboratory from patients with cancer may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors predict how patients will respond to treatment. PURPOSE: This research study is studying blood samples from patients with metastatic prostate cancer previously treated with bicalutamide and goserelin.

NCT ID: NCT01120236 Completed - Clinical trials for Prostate Adenocarcinoma

Bicalutamide and Goserelin or Leuprolide Acetate With or Without Cixutumumab in Treating Patients With Newly Diagnosed Metastatic Prostate Cancer

Start date: December 2010
Phase: Phase 2
Study type: Interventional

This randomized phase II trial is studying bicalutamide, goserelin, or leuprolide acetate to see how well they work when given with or without cixutumumab in treating patients with newly diagnosed metastatic prostate cancer. Androgens can cause the growth of prostate cancer cells. Antihormone therapy, such as bicalutamide, goserelin, or leuprolide acetate, may lessen the amount of androgens made by the body. Monoclonal antibodies, such as cixutumumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. It is not yet known whether bicalutamide, goserelin, or leuprolide acetate are more effective when given with or without cixutumumab in treating prostate cancer.

NCT ID: NCT01118741 Completed - Prostate Cancer Clinical Trials

Study of Recurrent Prostate Cancer With Rising Prostate Specific Antigen (PSA)

Start date: May 2010
Phase: N/A
Study type: Interventional

disulfiram is a DNA methyltransferase inhibitor that may provide benefit for patients with prostate cancer by restoring tumor suppressor genes.