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Liver Neoplasms clinical trials

View clinical trials related to Liver Neoplasms.

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NCT ID: NCT00997022 Completed - Clinical trials for Hepatocellular Cancer

Trial of Sorafenib in Hepatocellular Cancer (HCC) Transplant Patients

Start date: May 2009
Phase: Phase 1
Study type: Interventional

This Phase I study of sorafenib in high risk hepatocellular cancer patients after liver transplantation will study 24 subjects for about 5 years. Each subject will receive sorafenib for 6 months. Safety and effectiveness on the post transplant, high risk HCC patients will be studied.

NCT ID: NCT00994370 Completed - Liver Cancer Clinical Trials

Measurement of Pro-angiogenic Markers in Patients With Hepatic Metastases Undergoing SIRT

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

This study is being done to investigate the influence of giving radiation to the liver on tumors involving the liver. Investigator is specifically looking at this effect on the blood vessels within the tumor. This effect will be measured by studying substances in the blood that the tumors produce and that cause blood vessels to grow. The effects seen on these substances may help design other treatments to improve the results of the radiation used to treat these tumors.

NCT ID: NCT00987766 Completed - Pancreatic Cancer Clinical Trials

Gemcitabine Hydrochloride, Oxaliplatin, and Erlotinib Hydrochloride in Treating Patients With Advanced Biliary Tract Cancer, Pancreatic Cancer, Duodenal Cancer, or Ampullary Cancer

Start date: November 2009
Phase: Phase 1
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as gemcitabine hydrochloride and oxaliplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Erlotinib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving gemcitabine hydrochloride and oxaliplatin together with erlotinib hydrochloride may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of erlotinib hydrochloride when given together with gemcitabine hydrochloride and oxaliplatin in treating patients with advanced biliary tract cancer, pancreatic cancer, duodenal cancer, or ampullary cancer.

NCT ID: NCT00976898 Completed - Liver Cancer Clinical Trials

Proton Beam Irradiation for the Treatment of Unresectable Hepatocellular Cancer and Cholangiocarcinoma

Start date: August 2009
Phase: N/A
Study type: Interventional

In this study the investigators will be studying the effects of proton beam radiation therapy. This is a very accurate kind of treatment that has been shown to affect less normal tissue than a photon radiation beam. The accuracy allows the investigators to more safely increase the amount of radiation delivered to eliminate cancer. This accuracy will potentially reduce side effects that participants would normally experience using photon radiation therapy. The purpose of this study is to determine if radiation using proton beam therapy will kill the cancer cells in the participants liver.

NCT ID: NCT00969410 Completed - Liver Metastases Clinical Trials

A Pharmacodynamic Study of AV-299 (Formerly SCH 900105) in Subjects With Advanced Solid Tumors Who Have Liver Metastases

Start date: August 2009
Phase: Phase 1
Study type: Interventional

A pharmacodynamic study to evaluate the effect of AV-299 on exploratory pharmacodynamic markers in subjects with advanced solid tumors who have liver metastases. To evaluate safety and tolerability of AV-299 administered IV in subjects with advanced solid tumors who have liver metastases.

NCT ID: NCT00960609 Completed - Liver Tumors Clinical Trials

Communicating Veins Between Adjacent Hepatic Veins: an Intra-operative Ultrasound Study

Start date: January 2008
Phase: N/A
Study type: Observational

The search for communicating veins (CVs) between adjacent hepatic veins (HVs) has drawn its rationale from living donor liver transplantation (LDLT). Parenchymal sparing procedures although HVs are resected suggest that probably their presence is underestimated. Taking profit from new improvements in ultrasound technology the investigators aim to better estimate the rate of CVs in a consecutive series of patients in whom resection of one HV at caval confluence is needed.

NCT ID: NCT00960557 Completed - Neoplasm Metastasis Clinical Trials

Safety Study of Increasing Doses of Combretasatin A1 Diphosphate (OXi4503) as Monotherapy in Subjects With Hepatic Tumor Burden

OXi4503
Start date: July 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety and tolerability of OXi4503 in subjects with relapsed or refractory carcinomas with hepatic tumor burden.

NCT ID: NCT00957424 Completed - Lung Cancer Clinical Trials

Acceptability of Less Harmful Alternatives to Cigarettes

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

RATIONALE: A study that evaluates participants' beliefs about smokeless tobacco products and nicotine replacement therapy may be useful in helping smokers stop smoking. PURPOSE: This clinical trial is studying the acceptability of less harmful alternatives to cigarettes.

NCT ID: NCT00956930 Completed - Liver Cancer Clinical Trials

Chemoembolization Versus Radioembolization in Treating Patients With Liver Cancer That Cannot Be Treated With Radiofrequency Ablation Or Surgery

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

RATIONALE: Chemoembolization kills tumor cells by blocking the blood flow to the tumor and keeping chemotherapy drugs near the tumor. Radioembolization kills tumor cells by blocking the blood flow to the tumor and keeping radioactive substances near the tumor. It is not yet known which treatment regimen is more effective in treating patients with liver cancer. PURPOSE: This randomized phase II trial is studying radioembolization to see how well it works compared with chemoembolization in treating patients with liver cancer that cannot be treated with Radiofrequency Ablation or removed by surgery.

NCT ID: NCT00955097 Terminated - Liver Tumors Clinical Trials

Evaluation of Intra-operative Ultrasound Contrast Enhancement in the Evaluation of Liver Tumors

Definity®
Start date: May 2008
Phase: Phase 1
Study type: Interventional

The primary purpose of this study is to demonstrate the safety and effectiveness of using an intra-operative ultrasound contrast agent(Definity®) for the identification of known liver tumors.