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Carcinoma, Hepatocellular clinical trials

View clinical trials related to Carcinoma, Hepatocellular.

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NCT ID: NCT01506115 Completed - Clinical trials for Hepatocellular Carcinoma

Safety and Efficacy of Photodynamic Therapy for Bile Duct Invasion of Hepatocellular Carcinoma

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

The prognosis of patients with obstructive jaundice caused by hepatocellular carcinoma (HCC) is dismal even after biliary drainage; due to malfunction of the biliary drainage tube caused by hemobilia and/or tumor emboli. Photodynamic therapy (PDT) in hilar cholangiocarcinoma improves biliary drainage and prolongs survival. The aims of this study were to assess the safety and efficacy of PDT in unresectable HCC with bile duct invasion.

NCT ID: NCT01502410 Completed - Clinical trials for Papillary Thyroid Cancer

Sorafenib Tosylate in Treating Younger Patients With Relapsed or Refractory Rhabdomyosarcoma, Wilms Tumor, Liver Cancer, or Thyroid Cancer

Start date: January 2012
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well sorafenib tosylate works in treating younger patients with relapsed or refractory rhabdomyosarcoma, Wilms tumor, liver cancer, or thyroid cancer. Sorafenib tosylate may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth.

NCT ID: NCT01498952 Completed - Clinical trials for Unresectable or Metastatic Hepatocellular Carcinoma (HCC)

MEDI-573 in Combination With SOC in Unresectable or Metastatic HCC.

MEDI-573-1028
Start date: January 17, 2012
Phase: Phase 1
Study type: Interventional

A Phase 1b/2, open-label, randomized study to evaluate MEDI-573 in combination with standard of care in adult subjects with unresectable or metastatic hepatocellular carcinoma (HCC).

NCT ID: NCT01490203 Completed - Clinical trials for Carcinoma, Hepatocellular

Evaluation of Remnant Liver Function Using Primovist-enhanced MRI Before Resection/Ablation of Hepatocellular Carcinoma

LiFE
Start date: December 2011
Phase:
Study type: Observational

The purpose of this study is to determine whether the global and segmental hepatic uptake and excretion of Gd-EOB-DTPA on Gd-EOB-DTPA-enhanced liver MRI correlates with standard liver function test results in the patients with Hepatocellular Carcinoma (HCC) before major hepatic resection or radiofrequency ablation (RFA).

NCT ID: NCT01488487 Completed - Clinical trials for Advanced Adult Hepatocellular Carcinoma

Everolimus and Pasireotide (SOM230) in Patients With Advanced or Metastatic Hepatocellular Carcinoma

Start date: December 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to estimate the time to disease progression when everolimus and pasireotide are given together in patients with advanced or metastatic HCC who have not had any prior systemic therapy.

NCT ID: NCT01482520 Completed - Clinical trials for Hepatocellular Carcinoma

Genome-wide Association Study to Predict Treatment Response for Molecular Targeted Therapy in Hepatocellular Carcinoma and Renal Cell Carcinoma

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

All Hepatocellular carcinoma and Renal cell carcinoma patients who receive molecular targeted therapy will be candidates for the study. No additional treatment or intervention will be conducted except for blood sampling that will be limited to one time only. Blood samples (10 cc in volume) will be collected from all study participants once they provided written informed consent form. DNA will be extracted from peripheral blood samples using DNA isolation kit.

NCT ID: NCT01482442 Completed - Liver Carcinoma Clinical Trials

SorAfenib Versus RADIOEMBOLIZATION in Advanced Hepatocellular Carcinoma

SARAH
Start date: December 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether RADIOEMBOLIZATION with 90 Yttrium microspheres is more effective on overall survival in advanced Hepatocellular carcinoma (HCC) with or without portal venous obstruction and no extrahepatic extension than sorafenib which is now the standard treatment of advanced HCC.

NCT ID: NCT01481805 Completed - Clinical trials for Hepatocellular Carcinoma

Biomarker Analysis in Sorafenib Treated Hepatocellular Carcinoma Patients

Start date: January 14, 2010
Phase: N/A
Study type: Observational

To explore biomarkers predictive of clinical response to sorafenib in unresectable hepatocellular carcinoma using the Prometheus Platform To analyze expression and activation status of receptor tyrosine kinases in signal transduction pathways in FNA samples and circulating tumor cells. To identify negative predictive markers to sorafenib. To elucidate signal transduction pathway attributable to sorafenib resistance. To monitor changes in the RTK activation status during sorafenib treatment using circulating tumor cells. To analyze correlation between the quantity of circulating tumor cells and circulating endothelial cell precursors and treatment response to sorafenib.

NCT ID: NCT01474694 Completed - Adult Liver Cancer Clinical Trials

Accuracy Assessment for Computer-assisted Surgical Interventions of the Liver

CALS
Start date: October 2011
Phase: N/A
Study type: Observational

Preoperative image-guided data correlates with the actual intraoperative reality. Computer-assisted preoperative planning combined with intraoperative mapping of even very small lesions allows for improved accuracy during complete oncological resection / ablation. In the short- and long-term this possibly results in better patient outcome.

NCT ID: NCT01473121 Completed - Clinical trials for Hepatocellular Carcinoma

Hepatocellular Carcinoma Registry for Turkey (3K Trial)

Start date: August 13, 2012
Phase:
Study type: Observational

This registry study is national, multi-center, prospective study without any interventions to the treatment strategies and/or decisions of the investigators. It is designed in order to determine the general profile of HCC patients in Turkey. Socio-demographic characteristics, family history, medical history and treatment pattern of HCC patients will be evaluated.