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Prostatic Neoplasms clinical trials

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NCT ID: NCT00186420 Completed - Prostate Cancer Clinical Trials

Adjuvant Taxotere in Patients With High Risk Prostate Cancer Post Prostatectomy and Radiation

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

The purpose of this study is to evaluate time to progression (TTP) by PSA in patients with high risk prostate cancer after definitive therapy.

NCT ID: NCT00186108 Completed - Prostate Cancer Clinical Trials

A Pilot Study Evaluating Oral Triamcinalone in Patients With Androgen Independent Prostate Cancer

Start date: October 2002
Phase: Phase 1
Study type: Interventional

The primary purpose of this study is to evaluate the ability of oral triamcinalone given twice a day to patients with androgen independent prostate cancer to produce a sustained biochemical response. Secondary goals are to describe the safety and tolerability at this dose and schedule, to determine the time to sustained biochemical response, to determine the duration of biochemical response, to determine the time to disease progression.

NCT ID: NCT00183937 Completed - Prostate Cancer Clinical Trials

Study of Bortezomib and Docetaxel for Patients With Hormone Refractory Prostate Cancer

Start date: April 30, 2005
Phase: Phase 2
Study type: Interventional

This study is for patients who have been treated with surgical removal of the testes or hormone therapy (Lupron or Zoladex) and whose prostate cancer has worsened despite this treatment. PS 341 is a type of drug known as a "proteasome inhibitor." By inhibiting the "proteasome" in cancer cells, PS-341 alters the way those cells divide). We hope to learn whether this combination chemotherapy decreases cancer symptoms and tests (prostate specific antigen, also called PSA), and to determine how frequently serious side effects might occur with this treatment for this stage of prostate cancer.

NCT ID: NCT00183924 Completed - Clinical trials for Prostate Adenocarcinoma

Estramustine, Docetaxel, and Carboplatin for Patients With Hormone Refractory Prostate Cancer Progressing After Mitoxantrone-Based Chemotherapy.

Start date: March 2001
Phase: Phase 2
Study type: Interventional

This study is for patients with prostate cancer that is metastatic, progressive, and resistant to hormonal manipulation and mitoxantrone chemotherapy.Patients have previously been treated with surgical removal of the testes or hormone therapy, and subsequently with chemotherapy that included the drug, mitoxantrone (Novantrone). Patients will have prostate cancer that has worsened despite these treatments. We hope to learn whether the combination chemotherapy decreases cancer symptoms and tests, and to determine how frequently serious side effects occur with acceptable toxicity from the chemotherapy.

NCT ID: NCT00182741 Completed - Prostate Cancer Clinical Trials

Calcitriol, Mitoxantrone, and Prednisone in Treating Patients With Metastatic Prostate Cancer

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

RATIONALE: Calcitriol may cause prostate cancer cells to look more like normal cells, and to grow and spread more slowly. Drugs used in chemotherapy, such as mitoxantrone and prednisone, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. PURPOSE: This phase II trial is studying how well giving calcitriol together with mitoxantrone and prednisone works in treating patients with metastatic prostate cancer.

NCT ID: NCT00182624 Completed - Prostatic Neoplasms Clinical Trials

Magnetic Resonance Imaging to Evaluate Prostate Cancer

Start date: February 2, 2004
Phase: N/A
Study type: Observational

This study will determine whether scanning the prostate using special magnetic resonance imaging (MRI) techniques can detect prostate cancers with greater accuracy than other methods. MRI uses a strong magnet and radio waves to produce images of body tissues. Unlike many cancers, prostate cancer is difficult to see on most imaging studies like x-rays, computed tomography (CT) scans, and conventional MRI scans. This study will use a magnet twice as strong as the magnets commonly used in MRI tests. Patients 18 years of age and older with prostate cancer confirmed by prostate biopsy may be eligible for this study. Candidates are screened with a medical history, physical examination, and review of pathology reports. Participants undergo MRI of the prostate and possibly a biopsy of the prostate gland, as follows: Prostate MRI Before coming to the NIH Clinical Center for the biopsy, patients take a Fleets enema to empty the rectum of fecal matter. For the MRI, an endorectal coil (a tube containing a specially designed antenna) is placed in the rectum, which is just behind the prostate. The coil increases the amount of signal received by the MRI unit. Additional coils may be wrapped around the pelvis to further improve the quality of the scan. The patient lies on a stretcher that moves into the scanner. A catheter (plastic tube) is placed in an arm vein for injection of a contrast agent called gadolinium, which brightens the images. Patients may also be asked to breathe an oxygen-rich gas through a mask during the scan to test the use of oxygen as a contrast agent in MRI. Patients may be asked to repeat the MRI to test the reproducibility of the procedure. The repeat test is optional. Prostate Biopsy Depending on the MRI findings, patients may be asked to undergo a prostate biopsy to obtain a sample of tumor tissue. The tissue is obtained with a needle placed through the rectum. Medicines may be used to reduce pain during the biopsy and to reduce the chance of infection.

NCT ID: NCT00182052 Completed - Prostate Cancer Clinical Trials

Rosiglitazone (Avandia) vs. Placebo for Androgen Dependent Prostate Cancer

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

The purpose of this study it to learn the effects (good or bad) that rosiglitazone has on patients and their prostate cancer. This study is going to look at what effects rosiglitazone has on prostate specific antigen (PSA) levels.

NCT ID: NCT00181597 Completed - Prostate Cancer Clinical Trials

Trilostane for Androgen-Independent Prostate Cancer

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

The main purpose of this study is to test the safety of trilostane by looking at what effects, good and bad, it has on patients with androgen-independent prostate cancer.

NCT ID: NCT00181584 Completed - Prostate Cancer Clinical Trials

Zoledronic Acid to Prevent Bone Loss During Androgen Deprivation Therapy for Prostate Cancer

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

The primary objective of this study is to determine whether zoledronic acid (Zometa) given once annually increases bone mineral density in men receiving hormone therapy for prostate cancer.

NCT ID: NCT00181558 Completed - Prostate Cancer Clinical Trials

Atrasentan and Zometa for Men With Prostate Cancer Metastatic to Bone

Start date: December 2001
Phase: Phase 2
Study type: Interventional

The main purpose of this study is to look at the effects (good or bad) that Atrasentan given alone and Atrasentan given with Zometa has on levels of bone formation and bone destruction in men with prostate cancer that has spread to the bones.