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Neoplasm Metastasis clinical trials

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NCT ID: NCT00920504 Completed - Neoplasm Metastasis Clinical Trials

Pilot Study to Test the Feasibility and the Efficacy of the German Language Adapted PRO-SELF© Plus Pain Control Program

PEINCA
Start date: June 2009
Phase: N/A
Study type: Interventional

The purpose of this pilot study is to refine and test an advanced and adapted German version of the PRO-SELF© Plus Pain Control Program (PCP), an educational intervention directed at cancer pain patients and their families to enhance their pain self management abilities, and to calculate effect sizes for the planning of a sufficiently powered randomized controlled trial (RCT).

NCT ID: NCT00918645 Terminated - Prostate Cancer Clinical Trials

Calcium-41 (41Ca) Chloride Aqueous Solution in Diagnosing Patients With Prostate Cancer and Bone Metastasis

UCDCC#217
Start date: September 2009
Phase: N/A
Study type: Interventional

RATIONALE: Diagnostic procedures, such as radionuclide imaging using calcium-41 (41Ca) chloride aqueous solution, may help predict progressive disease in patients with prostate cancer and bone metastasis. PURPOSE: This clinical trial is studying how well calcium-41 (41Ca) chloride aqueous solution works in diagnosing patients with prostate cancer and bone metastasis.

NCT ID: NCT00918593 Withdrawn - Clinical trials for Ulcerated Cutaneous Metastases

Palliative Treatment of Ulcerated Cutaneous Metastases: Trial Between Electrochemotherapy and Radiotherapy

Start date: December 2009
Phase: Phase 2
Study type: Interventional

By applying short electric pulses to cells, the cell membranes can become permeabilised (electroporation). This can be used augment the effect of chemotherapy, by providing direct access to the cell cytosol. For the drug bleomycin, the enhancement of effect is several hundred fold, enabling once-only treatment. The investigators wish compare electrochemotherapy with radiotherapy when treating ulcerated cutaneous metastases up to 5 cm in diameter from any kind of histology.

NCT ID: NCT00917670 Completed - Uveitis Clinical Trials

Ultrastructural Changes of Trabeculectomy Specimens in Patients With Uveitic Secondary Glaucoma

Start date: May 2009
Phase: N/A
Study type: Observational

Ultrastructural analysis of trabeculectomy specimens of patients with uveitic secondary glaucoma. To evaluate morphological changes and to compare to primary open angle glaucoma patients.

NCT ID: NCT00914615 Completed - Liver Metastasis Clinical Trials

Stereotactic Body Radiation Therapy (SBRT) in Liver Metastasis (COLD 3)

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

This study is designed to see whether stereotactic body radiation therapy (SBRT) can reduce tumour size, slow progression of the disease, prolong life and improve quality of life. SBRT is concentrated focused radiation therapy delivered very precisely to the liver tumour. Presently, the treatment for unresectable liver metastases from colorectal cancer is most often chemotherapy or novel targeted therapy. These treatments may improve survival, but not control the metastases permanently; so new treatments are needed to control metastases. It is hoped that knowledge obtained from this study will improve our ability to treat patients with liver tumours that cannot be treated with surgery and other methods, and that SBRT may prove to be a treatment that can lead to long-term and permanent control of liver tumours for some patients.

NCT ID: NCT00910039 Terminated - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Sunitinib Malate After Stereotactic Radiosurgery in Treating Patients With Newly Diagnosed Brain Metastases

Start date: April 2009
Phase: Phase 2
Study type: Interventional

RATIONALE: Sunitinib malate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. PURPOSE: This phase II trial is studying how well sunitinib malate works after stereotactic radiosurgery in treating patients with newly diagnosed brain metastases.

NCT ID: NCT00908024 Terminated - Colorectal Cancer Clinical Trials

Combination Study of BMS-754807 and Erbitux® in Subjects With Advanced or Metastatic Solid Tumors

Start date: October 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The study is expected to identify a safe dose of BMS-754807 to be given in combination with a standard dose of cetuximab and the recommended dose or dose range for Phase II studies. The study is also intended to collect first data on the effects of the combination of BMS-754807 with cetuximab on tumors of patients with colorectal cancer or squamous cell cancer of the head and neck for whom cetuximab-containing therapies have not been effective

NCT ID: NCT00904553 Completed - Neoplasm Metastasis Clinical Trials

Study of Resection Combined With Stereotactic Radiosurgery for 1 to 3 Brain Metastases

Start date: January 14, 2009
Phase:
Study type: Observational

This study is to look more closely at the tumor removed during your surgery, and to follow your condition after your treatment. The purpose of this study is to determine what side effects are common or more rare from this treatment, how well the treatment has worked for you, and to track whether you develop other brain metastases.

NCT ID: NCT00899665 Completed - Prostate Cancer Clinical Trials

Proteases in Patients With Prostate Cancer That Has Spread to the Bone

Start date: July 2001
Phase: N/A
Study type: Observational

RATIONALE: Collecting and storing samples of bone marrow and tissue from patients to test in the laboratory may help the study of cancer. PURPOSE: This laboratory study is comparing proteases (enzymes that break down protein) in patients with prostate cancer that has spread to the bone with patients who do not have cancer that has spread to the bone.

NCT ID: NCT00899613 Recruiting - Metastatic Cancer Clinical Trials

Mesothelin and Osteopontin as Diagnostic Markers in Patients With Mesothelioma or Atypical Mesothelial Hyperplasia

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

RATIONALE: Studying levels of mesothelin and osteopontin in samples of blood from patients with mesothelioma or atypical mesothelial hyperplasia may help doctors identify biomarkers related to cancer. PURPOSE: This research study is looking at mesothelin and osteopontin as diagnostic markers in patients with mesothelioma or atypical hyperplasia.