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Carcinoma, Hepatocellular clinical trials

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NCT ID: NCT05677724 Recruiting - HBV Clinical Trials

Single-cell RNA Sequencing Resolves the Regulatory Role of HBV on the Hepatocellular Carcinoma Immune Microenvironment

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

In summary, with the help of single-cell sequencing technology, this study aims to focus on elucidating the influence of HBV-induced hepatocellular carcinoma cell metabolic changes on microenvironment remodeling. With the help of hepatocellular carcinoma microenvironment changes, this study provide a more accurate diagnosis and treatment method for HBV-induced hepatocellular carcinoma.

NCT ID: NCT05675462 Recruiting - Clinical trials for Hepatocellular Carcinoma

Oncolytic Virotherapy Plus PD-1 Inhibitor and Lenvatinib as Second-line or Later Therapy in Patients With Advanced Hepatocellular Carcinoma

Start date: March 1, 2023
Phase: Phase 1
Study type: Interventional

The objective of this study is to evaluate the safety/tolerability efficacy of oncolytic virotherapy combined with Tislelizumab plus lenvatinib as second-line or later therapy in patients with advanced hepatocellular carcinoma.

NCT ID: NCT05670561 Recruiting - Pain Clinical Trials

Effects of Esketamine on Acute Abdominal Pain After TACE in Patients With Hepatocellular Carcinoma

Start date: January 5, 2023
Phase: Phase 4
Study type: Interventional

Pain is the main complication after TACE(Transcatheter Arterial Chemoembolization) for hepatocellular carcinoma, and its pathogenesis is not clear.The pain may be related to partial liver tissue swelling after blocking the tumor blood supply artery embolization agent, transient hepatic swelling causing tension or strain on the liver capsule, and chemical irritation by the anticancer drug-Lipiodol mixture,the inadvertent embolization of normal organs and individual sensitivity to pain. Ketamine produces anesthetic and analgesic effects mainly by inhibiting NMDA receptor(N-methyl-D-aspartic acid receptor), and previous studies have shown that low concentrations of ketamine have obvious analgesic effects. Not only that, ketamine also produces analgesic effects by inhibiting opioid receptors via G-protein coupling. In addition, ketamine can bind to monoaminergic receptors in the central and peripheral nervous system, showing an anticholinergic effect and producing an antispasmodic effect. Ketamine also inhibits inflammatory pain by reducing nitric oxide production by inhibiting nitric oxide synthase. Esketamine is about three to four times more potent than ketamine. Therefore,esketamine requires a lower dose, about half the dose of ketamine, to produce anesthetic and analgesic effects, with fewer side effects.

NCT ID: NCT05667064 Recruiting - Clinical trials for Unresectable Hepatocellular Carcinoma

Imfinzi/Imjudo uHCC Japan PMS _ Japan Post-Marketing Surveillance (PMS) Study

Start date: May 10, 2023
Phase:
Study type: Observational

This investigation will be conducted to collect information of safety in patients with unresectable hepatocellular carcinoma (HCC) treated with the combination therapy of IMJUDO 25 mg, 300 mg and IMFINZI Intravenous Infusion 120 mg, 500 mg or with IMFINZI monotherapy under actual use in the post-marketing setting.

NCT ID: NCT05666271 Recruiting - Clinical trials for Hepatocellular Carcinoma

Radiofrequency Ablation for Hepatocellular Carcinoma Using Octopus MP Electrodes

Start date: August 29, 2022
Phase:
Study type: Observational

This study is to investigate the therapeutic effect and treatment results of radiofrequency ablation using the Octopus MP electrode capable of temperature monitoring and drug injection and a variable-length electrode for treatment of small hepatocellular carcinomas (≤ 3cm).

NCT ID: NCT05654896 Recruiting - Clinical trials for Antibiotic Prophylaxis

Prophylactic Antibiotic Use in Transarterial Chemoembolization for Hepatocellular Carcinoma

Start date: November 26, 2022
Phase: Phase 3
Study type: Interventional

This study aims to determine the effectiveness of prophylactic antibiotic use for TACE and occurrence of postoperative liver abscess. There would be two comparison groups. Current standard of care treatment at PKLI&RC (as per local guidelines) would be given to all patients receiving TACE for the intervention group or 'antibiotic group' (i.e., Inj. Ceftriaxone 1g, intravenous × stat). While no antibiotic would be given to the 'no antibiotic group'.

NCT ID: NCT05652920 Recruiting - Clinical trials for Hepatocellular Carcinoma

Ori-C101Chimeric Antigen Receptor (CAR) Modified T Cells for the Treatment of HCC

Start date: December 15, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

This is a Phase I, open-label, multi-center study to assess the safety, pharmacokinetics, and preliminary efficacy of GPC3-directed chimeric antigen receptor modified T cells injection (Ori-C101) in Advanced Hepatocellular Carcinoma(HCC).

NCT ID: NCT05644379 Recruiting - Clinical trials for Advanced Hepatocellular Carcinoma That Has Failed at Least One Prior Systemic Therapy

A Study Evaluating Cadonilimab Injection in Combination With Regorafenib for the Advanced Hepatocellular Carcinoma

Start date: November 25, 2022
Phase: Phase 1
Study type: Interventional

To evaluate the efficacy and safety of Cadonilimab Injection in combination with Regorafenib in the treatment of intermediate to advanced hepatocellular carcinoma that has failed at least one prior systemic therapy .

NCT ID: NCT05635279 Recruiting - Clinical trials for Hepatocellular Carcinoma

Effect of Nutritional Indices on the Prognosis of HCC Patients

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

Primary liver cancer has recently ranked among the leading causes of cancer death, with hepatocellular carcinoma (HCC) accounting for 75%-85% of these cases. In recent years, immune checkpoint inhibitors (ICIs) combined with tyrosine kinase inhibitors (TKIs) have achieved good results in the treatment of advanced HCC patients. So far, there is a lack of studies exploring the relationship between nutritional index and the prognosis of HCC patients treated with ICIs combined with TKIs, and there are few studies on the prognostic value of nutritional index in HCC patients treated with transarterial chemoembolization (TACE). This retrospective study aims to analyze the prognostic value of prognostic nutritional index(PNI),body mass index (BMI), psoas muscle index(PMI)and geriatric nutritional risk index (GNRI) in HCC patients who received ICIs combined with TKIs or TACE, and to provide reference for the selection of nutritional intervention programs for HCC patients.

NCT ID: NCT05631613 Recruiting - Clinical trials for Hepatocellular Carcinoma

Lipiodol-TACE With Idarubicin Based On a Specific Emulsion Ratio for Hepatocellular Carcinoma

Start date: December 28, 2022
Phase:
Study type: Observational [Patient Registry]

The purpose of this observational study is to evaluate properties of lipiodol-idarubicin emulsion mixed with the best regimen obtained in vitro study, including stability, viscosity,visibility under X-ray and deposition, in order to maximize the efficacy of idarubicin-cTACE for HCC.