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Adenocarcinoma of the Prostate clinical trials

View clinical trials related to Adenocarcinoma of the Prostate.

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NCT ID: NCT02203695 Active, not recruiting - Clinical trials for Adenocarcinoma of the Prostate

Randomized Salvage Radiation Therapy Plus Enzalutamide Post Prostatectomy

Start date: March 28, 2015
Phase: Phase 2
Study type: Interventional

The primary hypothesis of this study is that outcomes for patients with biochemically recurrent prostate cancer following radical prostatectomy will be improved by the addition of enzalutamide for 6-months compared to standard-of-care salvage radiation therapy to allow for further study in the definitive phase III setting. This study builds on the prior success of high-dose bicalutamide (for 24 months) when combined with salvage external radiation therapy (XRT), while using a newer more potent anti-androgen for a shorter duration of time (6 months) in an effort to minimize adverse effects.

NCT ID: NCT02176902 Active, not recruiting - Clinical trials for Adenocarcinoma of the Prostate

Low-Fat Diet and Fish Oil in Men on Active Surveillance for Prostate Cancer

Start date: November 1, 2014
Phase: N/A
Study type: Interventional

This randomized phase II trial will evaluate if a low omega-6, high omega-3 fat diet combined with fish oil has the potential to delay disease progression in patients with prostate cancer undergoing active surveillance.

NCT ID: NCT02023463 Active, not recruiting - Clinical trials for Adenocarcinoma of the Prostate

Enzalutamide, Radiation Therapy and Hormone Therapy in Treating Patients With Intermediate or High-Risk Prostate Cancer

Start date: April 2, 2014
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and best way to give enzalutamide, radiation therapy, and hormone therapy in treating patients with intermediate or high-risk prostate cancer. Androgens can cause the growth of prostate cancer cells. Antihormone therapy, such as enzalutamide, may lessen the amount of androgens made by the body. Radiation therapy uses high energy x rays to kill tumor cells. Giving enzalutamide, radiation therapy, and hormone therapy may be an effective treatment for prostate cancer.

NCT ID: NCT01949337 Active, not recruiting - Clinical trials for Adenocarcinoma of the Prostate

Enzalutamide With or Without Abiraterone and Prednisone in Treating Patients With Castration-Resistant Metastatic Prostate Cancer

Start date: January 22, 2014
Phase: Phase 3
Study type: Interventional

This randomized phase III trial studies enzalutamide to see how well it works compared to enzalutamide, abiraterone, and prednisone in treating patients with castration-resistant metastatic prostate cancer. Androgens can cause the growth of prostate cancer cells. Drugs, such as enzalutamide, abiraterone acetate, and prednisone, may lessen the amount of androgens made by the body.

NCT ID: NCT01682772 Active, not recruiting - Clinical trials for Adenocarcinoma of the Prostate

TOPARP: A Phase II Trial of Olaparib in Patients With Advanced Castration Resistant Prostate Cancer

TOPARP
Start date: July 2012
Phase: Phase 2
Study type: Interventional

This is an open-label, single arm, two part adaptive design phase II trial of Olaparib in patients with advanced castration resistant prostate cancer. The trial aims to evaluate the the anti-tumour activity of Olaparib in metastatic castration resistant prostate cancer, identify molecular signatures of tumour cells in responding and non-responding patients, and to identify predictive biomarkers of Olaparib response.

NCT ID: NCT01655836 Active, not recruiting - Prostate Cancer Clinical Trials

High-Dose Rate Brachytherapy and Stereotactic Body Radiation Therapy in Treating Patients With Prostate Cancer

Start date: October 4, 2012
Phase: Phase 1
Study type: Interventional

The first technology is called high dose rate brachytherapy. Brachytherapy is sometimes called internal radiation therapy. High dose rate brachytherapy is a procedure that involves temporarily placing radioactive material inside the patient's body for about 10-20 minutes. Then, the remainder of the radiation treatment will be given over a 3 week period using stereotactic body radiation therapy (SBRT). SBRT is a novel treatment modality that involves the delivery of very high individual doses of radiation to tumors with high precision. This allows the doctor to deliver the same amount of radiation in a much shorter time. The purpose of this study is to determine the safety of brachytherapy when combined with hypofractionated SBRT.

NCT ID: NCT01517451 Active, not recruiting - Clinical trials for Adenocarcinoma of the Prostate

Radiation and Androgen Ablation for Prostate Cancer

Start date: May 22, 2013
Phase: Phase 1/Phase 2
Study type: Interventional

A study to see how effective and tolerable radiation therapy along with androgen deprivation therapy is in treating prostate cancer.

NCT ID: NCT01402154 Active, not recruiting - Clinical trials for Adenocarcinoma of the Prostate

EPISPOT Detection of Circulating Prostate Cells Among Adenocarcinoma Patients

Start date: January 3, 2012
Phase:
Study type: Observational

The primary objective of this study is to evaluate the predictive value (in terms of remission) of a new technique for detecting circulating, functional, prostate cells among patients with localized adenocarcinoma of the prostate, and prior to any treatment.

NCT ID: NCT01255891 Active, not recruiting - Clinical trials for Adenocarcinoma of the Prostate

Adjuvant Androgen Suppression Plus Radiation Therapy for High-Risk Localized Adenocarcinoma Prostate

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

To evaluate the efficacy of LHRH agonist with adjuvant pelvic radiation therapy in post radical prostatectomy patients with high risk pathological features for failure. To determine the freedom from biochemical (maintenance of a PSA less than nadir + 2 ng/ml) and clinical progression rate at 5 years.

NCT ID: NCT00764166 Active, not recruiting - Clinical trials for Adenocarcinoma of the Prostate

A Prospective Randomized Phase III Study Comparing Hormonal Therapy +/-Docetaxel

RisingPSA
Start date: June 2003
Phase: Phase 3
Study type: Interventional

The primary objective was to evaluate the PSA (biochemical) progression-free survival (PFS) of high-risk metastasis-free PC patients, treated with LH-RH agonist for one year with or without docetaxel after prior radical prostatectomy (RP) or radiotherapy (RT). The study was powered at 80% to detect a 25% improvement in biochemical PFS for a total sample size estimated at 252 patients, with a two-sided type I error rate of 5% (non-parametric methods.