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Hepatocellular Carcinoma clinical trials

View clinical trials related to Hepatocellular Carcinoma.

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NCT ID: NCT04797884 Recruiting - Clinical trials for Hepatocellular Carcinoma

Electromagnetic Fields Versus Placebo For Child-Pugh A and B Patients With Advanced Hepatocellular Carcinoma

ARTEMIS
Start date: July 2023
Phase: Phase 2/Phase 3
Study type: Interventional

The primary goals of this study are to compare overall survival and quality of life in subjects with Child-Pugh A or B advanced hepatocellular carcinoma when treated with a device emitting radiofrequencies modulated at specific frequencies or with a device emitting unmodulated radiofrequencies.

NCT ID: NCT04796025 Recruiting - Clinical trials for Hepatocellular Carcinoma

TACE Combined With Sintilimab Plus Bevacizumab Biosimilar in Hepatocellular Carcinoma (BCLC-C Stage ): a Prospective Single-arm Phase II Clinical Study

T-Double
Start date: September 23, 2021
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of transcatheter arterial chemoembolization (TACE) combined with pd-1 antibody immunotherapy (Sintilimab) and anti-VEGF (Bevacizumab Biosimilar) in patients with advanced hepatocellular carcinoma (BCLC-C Stage).

NCT ID: NCT04792801 Recruiting - Clinical trials for Hepatocellular Carcinoma

PET TDM FDG-Choline as a Decision-making Tool for Routine Care on the Liver Transplant List for HCC

TEP CARE
Start date: June 22, 2021
Phase:
Study type: Observational

HCC is the most common malignant liver tumor for which liver transplantation is one of the pivotal curative treatments. The best possible selection of patients who are candidates for transplantation is essential in the current context of a shortage of transplants. Performing a PET CT scan is not currently recommended in the pre-liver transplant workup for HCC. However, PET CT using in a complementary manner the FDG and Choline tracers appears promising in the management of HCC in view of its wide use in oncology and its major diagnostic and prognostic contribution compared to conventional imaging. In order to address this issue, a prospective cohort study including patients from the University Hospital of Rouen and Lille with hepatocellular carcinoma meeting the criteria for indication of liver transplantation validated in SPC will be set up, the main objective of which will be to assess the decision-making contribution of PET TDM FDG and Choline in addition to conventional imaging in the pre-transplant assessment.

NCT ID: NCT04792463 Recruiting - Clinical trials for Hepatocellular Carcinoma

Frequency and Clinical Phenotype of BAP1 Hereditary Predisposition Syndrome

Start date: March 3, 2015
Phase:
Study type: Observational

This research will have a significant impact on the overall management of those cancer patients and their family members who are at risk for hereditary cancer due to germline inactivation of BAP1. Our study will ultimately facilitate the development of novel screening, prevention and treatment strategies for these individuals with the syndrome. Because the vast majority of UM develop in pre-existing nevi, characterization of individuals at high risk for development of UM will allow closer screening and earlier intervention which would improve the treatment outcome not only for retaining vision but also for overall survival. Similarly in patients with germline BAP1 mutation CM develops in premalignant atypical melanocytic lesions and careful follow up of these patients will improve the outcome of their disease. In addition this study could have impact on the management of patients with personal and/or family history of several other cancers reported in patients with germline BAP1 mutation such as mesothelioma, renal cell carcinoma, cholangiocarcinoma, hepatocellular carcinoma, meningioma and basal cell carcinoma.

NCT ID: NCT04791735 Recruiting - Clinical trials for Hepatocellular Carcinoma

Value of the Laparoscopic Approach in the Surgical Management of Resectable Hepatocellular Carcinoma

LapCHC
Start date: May 21, 2021
Phase: N/A
Study type: Interventional

Hepatocellular carcinoma treated by laparotomy or laparoscopic Multicenter prospective, open, superiority, controlled, randomized, clinical trial The primary objective of the study will be to demonstrate the superiority of the laparoscopic approach over the open approach in reducing postoperative morbidity in HCC patients. Postoperative morbidity will be assessed using the Comprehensive Complication Index (CCI) within 90 days postoperatively or at any time during hospitalization

NCT ID: NCT04791176 Active, not recruiting - Clinical trials for Hepatocellular Carcinoma

Phase II Study of Concurrent Lenvatinib and Radiotherapy for Advanced HCC

Start date: April 12, 2021
Phase: Phase 2
Study type: Interventional

This is a single-arm, open-label study performed at our hospital, patients with progression hepatocellular carcinoma (HCC) met inclusion criteria will be enrolled. Patients received oral lenvatinib 12mg/day (for patients≥60 kg) or 8 mg/day (for patients<60kg ) before local radiotherapy 8 weeks, large lesions were treated with IMRT for 40-60gy / 20-30f. Combined therapy will be taken until unacceptable treatment-related toxicities occurred or disease progression.

NCT ID: NCT04780802 Completed - Clinical trials for Hepatocellular Carcinoma

Balloon Assisted Transarterial Therapy for Hepatocellular Carcinoma

Start date: May 1, 2022
Phase: N/A
Study type: Interventional

To prove the treatment concept of the use of balloon assistance in transarterial therapy for HCC.

NCT ID: NCT04780789 Completed - Clinical trials for Hepatocellular Carcinoma

Volumetric Analysis of Hepatocellular Carcinoma After Transarterial Chemoembolization

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

The application of transarterial chemoembolisation (TACE) with drug-eluting beads in patients with hepatocellular carcinoma and its response to the treatment will be observed. The registry has the following objectives: To assess the response to the treatment by standard methods and volumetric analysis as well as trying to determine any predictive response factors To determinate interobserver variability of the methods.

NCT ID: NCT04780217 Active, not recruiting - Colorectal Cancer Clinical Trials

Intravenous T3011 Given as a Single Agent and in Combination With Other Therapy in Subjects With Advanced Solid Tumors

Start date: August 10, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

A Phase 1/2a Open-Label Dose Escalation and Dose Expansion Study of T3011 when Administered Intravenously as a Single Agent and in Combination with Other Therapy in Subjects with Advanced Solid Tumors

NCT ID: NCT04777942 Recruiting - Clinical trials for Hepatocellular Carcinoma

Neo-TACE-HAIC for High-risk BCLC A Stage HCC (NeoconceptA)

Start date: February 20, 2021
Phase: N/A
Study type: Interventional

Hepatocellular carcinoma (HCC) patients is a common disease in the East Asia. Although resection was recommend for early stage (BCLC A stage) patients according to the BCLC (Barcelona clinical liver cancer) system, increasing studies suggested that preoperative transarterial therapy may decrease the recurrence risk for those with high-risk factors. However, the clinical value is still undertermined. Recently, FOLFOX (Oxaliplatin and 5-fluorouracil) based hepatic artery infusion chemotherapy (HAIC) exhibited high response rate for unresectable HCC. Pilot study showed TACE combined HAIC (TACE-HAIC) had better tumor response, with low progression disease rate. Whether TACE-HAIC would improve survival for BCLC A stage patients with high-risk factors is need to further to study. A randomized clinical trial compared neo-TACE-HAIC with surgery versus surgery alone is aimed to answer this question.