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Neoplasm Metastasis clinical trials

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NCT ID: NCT00184275 Completed - Melanoma Clinical Trials

Characterization of Brain Metastases

Start date: May 2005
Phase: N/A
Study type: Observational

The purpose is to characterize tumour biological markers in brain metastases tissue from patients with different primary tumour by using ex vivo techniques as high-resolution magic angle spinning MR spectroscopy and micro array.

NCT ID: NCT00182754 Completed - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Octreotide in Treating Patients With Cancer-Related Malignant Ascites

Start date: October 2005
Phase: Phase 3
Study type: Interventional

RATIONALE: Octreotide may be an effective treatment for malignant ascites. It is not yet known whether octreotide is more effective than a placebo in treating malignant ascites. PURPOSE: This randomized phase III trial is studying octreotide to see how well it works compared to placebo in treating patients with cancer-related malignant ascites.

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.

NCT ID: NCT00178243 Completed - Neoplasm Metastasis Clinical Trials

Feasibility of Treatment of Cancer Involving the Liver With High Dose Radiation

Start date: n/a
Phase: Phase 1/Phase 2
Study type: Interventional

A study is being conducted by the University of Rochester Cancer Center (URCC) in which patients with liver cancer will be treated with high dose conformal radiation therapy. This type of radiation uses new techniques which aim the radiation to the sites of disease allowing the tumor to receive a high dose and the surrounding normal liver tissue to receive a low enough dose that the normal tissue should remain free from injury. The purpose of the study is to determine if the conformal radiation therapy is safe, tolerable and effective in treating liver cancer and to determine the side effects caused by this treatment. A second objective is to determine if the levels of a special type of protein (called cytokines) found in the blood are related to this treatment.

NCT ID: NCT00172003 Completed - Neoplasm Metastasis Clinical Trials

Effect of Zoledronic Acid in Patients With Renal Cell Cancer and Bone Metastasis

Start date: September 2004
Phase: Phase 4
Study type: Interventional

It is the aim of this clinical study to evaluate the skeletal-related event rate under therapy with zoledronic acid in patients with renal cell cancer having at least one cancer-related bone lesion.

NCT ID: NCT00171964 Completed - Pain Clinical Trials

Efficacy and Tolerability of Zoledronic Acid With Radiotherapy in Pts With Advanced Osteolytic Bone Lesions

Start date: May 2002
Phase: Phase 4
Study type: Interventional

It is the aim of this multicentric clinical study to assess the efficacy and tolerability of zoledronic acid in combination with radiotherapy in patients with advanced osteolytic bone lesions in terms of the reduction of pain and analgesic consumption.

NCT ID: NCT00171873 Completed - Clinical trials for Neuroendocrine Tumors

Antiproliferative Effect of Octreotide in Patients With Metastasized Neuroendocrine Tumors of the Midgut

Start date: September 2001
Phase: Phase 3
Study type: Interventional

Placebo-controlled prospective randomized phase III study to investigate the antiproliferative effect of octreotide in patients with metastasized neuroendocrine tumors of the midgut

NCT ID: NCT00171587 Completed - Neoplasm Metastasis Clinical Trials

Study of the Safety, Tolerability, Pharmacokinetics, and Anti-tumor Effects of Vatalanib in Combination With Capecitabine in Patients With Advanced Cancer

Start date: May 2002
Phase: Phase 1/Phase 2
Study type: Interventional

The objective of this study is to assess the safety, tolerability, dose limiting toxicity, and maximum tolerated dose of vatalanib administered orally once daily in combination with capecitabine in patients with advanced cancer. The study is also designed to determine the effect of vatalanib on the pharmacokinetics of capecitabine and the effect of capecitabine on the pharmacokinetics of vatalanib, and to describe the anti-tumor activity of this combination regimen.

NCT ID: NCT00168155 Completed - Liver Metastases Clinical Trials

Study of 5-FU + Leucovorin + CPT-11 in Patients With Resectable Liver Metastases From Colorectal Adenocarcinoma

Start date: January 2002
Phase: Phase 2
Study type: Interventional

When colon or rectal cancer has spread to the liver, the cancer in the liver can sometimes be removed surgically. However, the cancer has a chance or reoccurring in the liver or elsewhere in the body. This study will determine if giving chemotherapy treatment before the surgery can reduce the chances that the cancer will come back.

NCT ID: NCT00165568 Completed - Colorectal Cancer Clinical Trials

Using Positron Emission Tomography to Evaluate the Effects of Bevacizumab on Intra-tumoral Pharmacokinetics of 5-fluorouracil in Metastatic Colorectal Cancer

Start date: July 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate whether bevacizumab helps 5-Fluorouracil (5-FU) be delivered to the tumor more efficiently. Bevacizumab has been shown to inhibit the formation of new blood vessels in tumors and works best in combination with drugs that require blood vessels for transportation. Based on other experiments, bevacizumab may work by improving the transportation of other drugs to the tumor.