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Carcinoma, Hepatocellular clinical trials

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NCT ID: NCT00162669 Recruiting - Clinical trials for Hepatocellular Carcinoma

Bevacizumab in Advanced Hepatocellular Carcinoma

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

Primary liver cancer (hepatocellular carcinoma) is the fifth most common malignant disorder, with an increasing incidence in Europe and the USA as a result of the high prevalence of hepatitis C. Most patients are not suitable for potentially curative treatment. There is no standard palliative treatment for patients with advanced hepatocellular carcinoma (HCC), as no drug has been demonstrated to be efficient in this disease in terms of survival. The use of anti-vascular agents might be a promising approach in view of the highly vascular nature of this tumor. The aim of this phase II trial is to evaluate the potential benefit of bevacizumab in terms of disease control rate, progression-free and overall survival in adult patients with advanced primary liver cancer. Bevacizumab is an angiogenesis inhibitor already successfully used in patients with colorectal and renal cancers.

NCT ID: NCT00155272 Recruiting - Clinical trials for Hepatocellular Carcinoma

Radiotherapy Plus Thalidomide in Locally Advanced Hepatocellular Carcinoma

Start date: March 2005
Phase: Phase 1/Phase 2
Study type: Interventional

This is a pilot study of concomitant radiotherapy and thalidomide for patients with locally advanced HCC.Besides toxicity and efficacy, mechanistic studies including dynamic contrast enhanced MRI and serum cytokines will be evaluated.

NCT ID: NCT00155103 Recruiting - Hepatitis B Clinical Trials

Effect of Polymorphisms in the IL-1 Gene Complex on the Development of Chronic Hepatitis and Hepatocellular Carcinoma

Start date: August 2004
Phase: N/A
Study type: Observational

The purpose of this study is to determine the effect of polymorphisms in the IL-1 gene complex on the development of chronic hepatitis and hepatocellular carcinoma.

NCT ID: NCT00154544 Recruiting - Clinical trials for Hepatocellular Carcinoma

Searching for the Liver Cancer-Related Biomarkers

Start date: August 2004
Phase: Phase 1
Study type: Observational

Hepatocellular carcinoma (HCC) has been the leading cause of cancer death in Taiwan. About 6000-8000 people died of this cancer every year in Taiwan. Though regular sonographic examination can early detect small HCC and there are many therapeutic modalities for HCC, the therapeutic results remains unsatisfactory. Though Alpha-fetoprotein (AFP) and des-γ-carboxy prothrombin (DCP) are used as the tumor markers for diagnosis of HCCs, these two markers are not good enough for the early detection of small HCCs. To improve the survival, further investigations of the early diagnostic markers are still needed. In this current project, we applied the proteomic method to identify the HCC biomarkers.

NCT ID: NCT00154531 Recruiting - Clinical trials for Hepatocellular Carcinoma

Identification of Biomarkers Associated With Human Hepatocellular Carcinoma by SELDI

Start date: August 2004
Phase: N/A
Study type: Observational

Hepatocellular carcinoma (HCC) has been the leading cause of cancer death in Taiwan. Though Alpha-fetoprotein (AFP) and des-γ-carboxy prothrombin(DCP) are used as the tumor markers for diagnosis of HCCs. Thus, these two markers are not good enough for the early detection of small HCCs. To improve the survival, further investigations of the early diagnostic markers are still needed. SELDI is a proteomic profiling techniques in biomarker discovery. Its approach has been successfully used to identify biomarkers of various cancers, such as prostate cancer, bladder cancer, ovarian cancer, lung cancer, colon cancer, breast cancer and pancreatic cancer. In this current project we will apply the SELDI technique to identify the HCC biomarkers. Sera samples from the HCC patients and relevant controls will be collected. We hope that we can find the new HCC biomarkers. If biomarkers of HCC are identified, this can be used to clinical application for the possible early detection of HCCs.