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HCC clinical trials

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NCT ID: NCT05781568 Recruiting - NAFLD Clinical Trials

Use of Blood Biomarkers for the Early Diagnosis of Hepatocellular Carcinoma (HCC)

GALAD
Start date: February 24, 2023
Phase:
Study type: Observational

The objective of this observational study is to evaluate the clinical utility of the combined assay of 3 biomarkers: α-FP, α-FP-L3 and DCP (simultaneously measured by µTASWakoTM i30 automated in vitro diagnostic system) in high-risk subjects to develop this neoplasm. In particular, it aims to: - Evaluate the clinical utility of the combined use of α-FP, α-FP-L3 and DCP in predicting the onset of HEPATOCARCINOMA (HCC); - Evaluate the performance of GALAD and GALADUS scores in the early diagnosis of HCC; - Evaluate the association between the levels of the three biomarkers (individually and in combination with each other) and the stage of HCC

NCT ID: NCT05637788 Active, not recruiting - HCC Clinical Trials

Artificial Intelligence and Hepatocellular Carcinoma

ARTIHCC
Start date: July 1, 2021
Phase:
Study type: Observational

To identify new relevant biomarkers for HCC patients and their risk of recurrence. Radiomics data and computer-vision data will be explored for their ability to predict the presence of particular pathological signs of aggressiveness (microvascular invasion and satellitosis), and the prognosis after surgery.

NCT ID: NCT05592171 Recruiting - HCC Clinical Trials

Occlusafe® Assisted MW Alone or With DEB-TACE Compared to MW With DEB-TACE in the Treatment of HCC

SEASON-HCC
Start date: October 17, 2022
Phase: N/A
Study type: Interventional

The goal of this Interventional Study is to compare the efficacy profile and safety of three treatments in patients with HCC nodule. Patients will be randomly divided in three arms: 1. Occlusafe assisted MWA+ DEB-TACE 2. Occlusafe assisted MWA 3. MWA+ DEB-TACE The primary objectives are evaluate the safety of the three treatments; evaluate the effectiveness of treatments one month after the procedure (defined as complete ablation of macroscopic tumor at one month of follow-up), verifying the possible superiority of arm 1 and arm 2 compared to arm 3. The secondary objective is: time to local disease recurrence.

NCT ID: NCT05581004 Recruiting - Gastric Cancer Clinical Trials

A Study to Evaluate the Safety, Pharmacokinetics, and Activity of RO7502175 as a Single Agent and in Combination With Atezolizumab in Participants With Locally Advanced or Metastatic Solid Tumors

Start date: October 20, 2022
Phase: Phase 1
Study type: Interventional

This is a first-in-human study to evaluate the safety, tolerability, pharmacokinetics (PK), and anti-tumor activity of RO7502175 when administered as a single agent and in combination with atezolizumab in adult participants with locally advanced or metastatic solid tumors, including non-small-cell lung cancer (NSCLC), head and neck squamous cell carcinoma (HNSCC), melanoma, triple-negative breast cancer (TNBC), esophageal cancer, gastric cancer, cervical cancer, urothelial carcinoma (UC), clear cell renal cell carcinoma (RCC) and hepatocellular carcinoma (HCC). Participants will be enrolled in 2 stages: dose escalation and dose expansion.

NCT ID: NCT05544253 Recruiting - Clinical trials for Hepatocellular Carcinoma

Safety and Efficacy of Mitomycin C-based HIPEC After srHCC and PM of HCC

Start date: October 1, 2022
Phase: Phase 2/Phase 3
Study type: Interventional

Hepatocellular carcinoma (HCC) is featured by the spontaneously rupture when suffering severe cirrhosis and intratumoral overpressure. It is a fatal complication with an acute mortality. Importantly, it is served as an independent risk factor for peritoneal metastasis (PM) of HCC with poor prognosis. The systematic agents effective to extrahepatic lesions confers modest efficacy towards PM. HIPEC, as a novel strategy, has been proved by overwhelming studies that it is effective to peritoneal malignant tumors. However, there is absence of prospective study of HIPEC efficacy towards HCC.

NCT ID: NCT05471674 Completed - Clinical trials for Hepatocellular Carcinoma

Neoadjuvant Anti-PD1 in HCC

Start date: July 3, 2020
Phase: Phase 2
Study type: Interventional

This is a phase 2, single-arm trial designed to assess the clinical benefit of treatment with nivolumab administered in patients with untreated, borderline resectable HCC.

NCT ID: NCT05458115 Not yet recruiting - HCC Clinical Trials

Clinical Study of MRD Recurrence Monitoring After Surgical Resection of Hepatocellular Carcinoma

Start date: September 30, 2022
Phase:
Study type: Observational

ctDNA-based liquid biopsy can better detect the presence of MRD before imaging and serological markers, and is suitable for postoperative MRD and recurrence monitoring, which has been clinically validated in several cancer types such as lung cancer and intestinal cancer. However, there is no systematic comparative study of postoperative MRD and recurrence monitoring based on ctDNA testing in hepatocellular carcinoma. A prospective multicenter observational clinical study is proposed to evaluate the use of liquid biopsy based on ctDNA NGS assay in surgical evaluation, MRD and molecular recurrence state monitoring after radical resection of hepatocellular carcinoma, and to compare with imaging and serological findings with the aim of early detection of disease recurrence or metastasis and more survival benefits for patients.

NCT ID: NCT05450874 Completed - HCC Clinical Trials

A Novel MSE Score to Predict rHCC Patients

Start date: February 1, 2010
Phase:
Study type: Observational

Develop and validate a novel scoring system based on pathological factors to predict the postoperative survival of patients with rHCC.Patients with rHCC who underwent hepatectomy were recruited from two hospitals.Exploring whether this scoring system is related to prognosis

NCT ID: NCT05402644 Completed - Portal Hypertension Clinical Trials

Hepatectomy for Early-stage HCC Patients With CSPH

Start date: December 1, 2009
Phase:
Study type: Observational

Clinically significant portal hypertension (CSPH) can affect the surgical prognosis of early-stage (BCLC stage A) HCC. An additional stage, such as the BCLC stage A-B, can be considered.

NCT ID: NCT05401890 Not yet recruiting - HCC Clinical Trials

Association Between Serum Ferritin Level and Severity of Liver Disease and Development of HCC in Cirrhotic Patients

Start date: August 1, 2022
Phase:
Study type: Observational

Association between serum ferritin level and severity of liver disease and development of HCC in cirrhotic patients .