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Carcinoma, Hepatocellular clinical trials

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NCT ID: NCT03702998 Completed - HIV Infections Clinical Trials

Hepatocellular Carcinoma in HIV-infected Individuals in Asian Population

Start date: December 1, 2018
Phase:
Study type: Observational

This is a retrospective study, all HIV-infected individuals followed up at the three designated HIV clinics in Hong Kong with and without HBV and/or HCV co-infection will be included in the analysis. The incidence and mortality of HCC among HIV-infected individuals with and without HBV/HCV co-infection in an Asian population will be determined.

NCT ID: NCT03699657 Completed - Clinical trials for Hepatocellular Carcinoma

Dual and Single Switching Monopolar RFA Using Separable Clustered Electrode for Treatment of HCC

Start date: December 15, 2014
Phase: N/A
Study type: Interventional

This study was conducted to prospectively compare the efficacy, safety and mid-term outcomes of dual-switching monopolar (DSM) radiofrequency ablation (RFA) with those of conventional single-switching monopolar (SSM) RFA in the treatment of hepatocellular carcinoma (HCC).

NCT ID: NCT03663114 Completed - Clinical trials for Carcinoma, Hepatocellular

A Post-marketing Observational Study on Risk Factors for Hepatic Encephalopathy in Participants With Unresectable Hepatocellular Carcinoma

Start date: July 2, 2018
Phase:
Study type: Observational

This study is a post-marketing observational study of lenvatinib in participants with unresectable hepatocellular carcinoma. The primary objective of this study is assessment of risk factors for hepatic encephalopathy.

NCT ID: NCT03648073 Completed - Clinical trials for Hepatocellular Carcinoma

[68Ga]DOTATATE-PET/MRI in Hepatocellular Carcinoma

Start date: January 30, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

There is great need for new therapeutic options for patients with hepatocellular carcinoma (HCC). This proposal will assess the feasibility of a novel theranostic approach to HCC using [68Ga]DOTATATE, a recently approved positron emission tomography (PET) ligand for imaging somatostatin receptor (SSTR) positive tumors. In this study, we will use [68Ga]DOTATATE to determine the percentage of HCCs that express adequate levels of SSTR for treatment with targeted radionuclide therapy (TRT) using the therapeutic SSTR ligand [177Lu]DOTATATE. This radionuclide therapy was FDA approved in January 2018 for treating neuroendocrine tumors (NETs) arising from the gastrointestinal tract, but its use in HCC has not yet been explored. In the long term, we envision using [68Ga]DOTATATE-PET to identify HCC patients with adequate SSTR expression for TRT using [177Lu]DOTATATE. Liver transplantation is the only curative therapy for HCC and is an option for a selected subset of HCC patients. For those who are not candidates for transplantation, locoregional therapies with limited efficacy are available such as percutaneous ablation, arterial chemoembolization, and Y-90 microsphere radionuclide therapies. There are few options for patients who progress or are not candidates for these therapies. The first line systemic therapy is sorafenib, a tyrosine kinase inhibitor. Sorafenib is often not well tolerated due to its side effects and there is need for additional systemic treatments. Multiple tissue-based studies demonstrate SSTR positivity in 20-50% of HCCs.[1-3] However, the fraction of HCCs have high enough levels of SSTR for [177Lu]DOTATATE therapy has not yet been assessed. This research plan is a critical prerequisite for determining the feasibility of this theranostic approach to treating HCC. If we obtain positive results, these data will be critical for designing a combined imaging and therapeutic study in HCC using DOTATATE.

NCT ID: NCT03636620 Completed - Clinical trials for Hepatocellular Carcinoma

TACE Combined With RFA/MV Treatment in Hepatocellular Carcinoma Beyond Milan Criterial

TACE+RFA
Start date: June 2013
Phase: Phase 3
Study type: Interventional

This study was designed to evaluate the effectiveness of radiofrequency /microwave ablation in patients with hepatocellular carcinoma beyond Milan Criteria.

NCT ID: NCT03630068 Completed - Clinical trials for Hepatocellular Carcinoma

Computer-assisted Tumor Ablation for Patients With Liver Cancer

Start date: January 1, 2015
Phase:
Study type: Observational

In patients with primary liver cancer arising from the liver cells, several treatment options are available according to the stage of the disease. Thermal ablation is a treatment modality using the deposition of thermal energy via an ablation probe to locally destroy the tumor tissue. It has been accepted as being equally effective as surgical resection in patients with very small tumors, as well as for patients with more advanced disease who are not surgical candidates or who are awaiting liver transplantation. Treatment success of thermal ablation is linked to the completeness of the tumor ablation and thus to the precision with which the ablation probes can be placed within the tumors. In recent years, novel computer-assister technology has been introduced to augment accuracy in ablation probe positioning, and first reports describing the safety and efficiency of these procedures have been described in the literature. However, very few works describe the oncological outcomes of patients when using this technology for thermal ablation. In this study, the investigators aim to describe local tumor control and the oncological follow-up of patients when using computer-assisted technology for thermal ablation of liver cancer.

NCT ID: NCT03628651 Completed - Clinical trials for Hepatocellular Carcinoma

Blood Sample Collection to Evaluate Biomarkers for Hepatocellular Carcinoma

Start date: April 2, 2018
Phase:
Study type: Observational

The primary objective of this study is to obtain de-identified, clinically-characterized whole blood specimens for use in developing and evaluating the performance of new biomarker assays for detection of hepatocellular carcinoma (HCC).

NCT ID: NCT03602703 Completed - Clinical trials for Drug-Induced Liver Injury

Immune Responses in Hepatocellular Carcinoma Patients After Treatment With Direct Acting Antiviral Drugs

Start date: July 1, 2018
Phase:
Study type: Observational

Case control Study to assess the difference of immune cell responses between patients with chronic HCV- related liver cirrhosis who develop HCC after treatment with DAAs and those who do not develop HCC

NCT ID: NCT03595345 Completed - Liver Cancer Clinical Trials

A Worldwide Score for Hepatocellular Cancer and Liver Transplantation

TRAIN-SCORE
Start date: December 15, 2016
Phase:
Study type: Observational

The present study has been developed with multiple aims: 1) to refine available models for liver transplantation which would be able to cover the fate of HCC candidates from an ITT point of view; 2) to develop such an approach on cohorts coming from both Eastern and Western countries; 3) to maintain simplicity of use; 4) to provide individual prognostication taking into account different causes of death, through a competing-risk model; 5) to provide an external validation on cohorts coming from both Eastern and Western countries. All these aims converge at providing a comprehensive and useful assessment suitable for both candidates selection and allocation priority.

NCT ID: NCT03594188 Completed - Clinical trials for Hepatocellular Carcinoma

Effects of Anesthetic Methods on Hepatic Cancer Cell Malignancy

Start date: July 23, 2018
Phase: N/A
Study type: Interventional

Numerous studies found that anesthetic methods can influence the recurrence of tumor and the overall survival of patients after primary cancer surgery. Radiofrequency (RF) ablation is now widely used in clinic for treatment of hepatocellular carcinoma (HCC). Currently, diverse anesthetic methods, including general anesthesia (GA), epidural anesthesia and local anesthesia (LA), are used for RF ablation surgery. Using serum from HCC surgery patients randomized to receive either GA or LA during surgery, we investigated the effects of anesthetic methods on proliferation, migration and metastasis in HepG2 hepatic cancer cells in vitro.