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Primary Liver Cancer clinical trials

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NCT ID: NCT06430983 Not yet recruiting - Clinical trials for Primary Liver Cancer

Recurrent Liver Cancer: Reconceptualization and Reevaluation

Start date: July 1, 2024
Phase:
Study type: Observational [Patient Registry]

The goal of this observational study is to determine if a specific protein can serve as a novel indicator for the recurrence of liver cancer. The study will focus on recurrent liver cancer patients and compare participants to primary liver cancer patients as controls. The primary purpose is to assess whether the elevated levels of this protein can be used to monitor the recurrence of liver cancer. The main questions it aims to answer are: Is the levels of the protein significantly elevated in recurrent liver cancer patients compared to primary liver cancer patients? Can the protein be used as a reliable biomarker for the early detection of liver cancer recurrence? Researchers will compare the protein levels in the following groups: 50 recurrent liver cancer patients (training set) with abnormally high levels of the protein. 250 recurrent liver cancer patients (validation set) to confirm the protein's elevation in a separate cohort. Participants will be required to: - Provide blood samples for protein analysis. - Undergo regular follow-up visits for monitoring and data collection. - Allow access to their medical records for relevant clinical information.

NCT ID: NCT05986383 Not yet recruiting - Clinical trials for Primary Liver Cancer

Multi-center Clinical Study on the Decision Tree of Precision Hepatectomy in China Precision Hepatectomy Decision Tree

Start date: August 2023
Phase:
Study type: Observational [Patient Registry]

Liver failure (PHLF) after hepatectomy is a relatively serious postoperative complication. Previous studies have shown that liver reserve function is related to PHLF. The "Chinese expert consensus decision tree for hepatectomy" implemented recommends different surgical methods according to the liver function of patients and the standardized residual functional liver volume ratio, so as to achieve accurate hepatectomy and prolong the survival of patients. In the retrospective study, it showed the safety and effectiveness of the decision tree under the condition of extended hepatectomy indications, but it lacked prospective research to evaluate. Therefore, this study intends to evaluate the safety and effectiveness of hepatectomy under the guidance of Chinese expert consensus decision tree through prospective research.

NCT ID: NCT05353894 Not yet recruiting - Clinical trials for Primary Liver Cancer

Effect of Food and Formulation on the Pharmacokinetics, Safety, and Tolerability of GNS561 After One Single Dose (50 and 200mg) in Healthy Volunteers

Start date: May 2, 2022
Phase: Phase 1
Study type: Interventional

GNS561 is a drug used in preliminary phase 1b study for treatment of patients with primary and secondary liver cancer. The formulation used was oral capsule.The objective of this study in healthy volunteers is to compare pharmacokinetics, safety and tolerability of different formulations (tablets and capsules) and dosage (50 and 200mg) of GNS561 after single oral administration in first part and to evaluate the food effect on pharmacokinetics in second part.

NCT ID: NCT03178929 Not yet recruiting - Clinical trials for Primary Liver Cancer

Effect of SAMe Treatment on Recurrence After Radical Treatment of Primary Hepatic Carcinoma

Start date: July 1, 2017
Phase: N/A
Study type: Interventional

The aim of this study is to explore the effect of SAMe on recurrence after radical treatment of Primary liver cancer.

NCT ID: NCT02327819 Not yet recruiting - Clinical trials for Primary Liver Cancer

The Effect of Branched-chain Amino Acid (BCAA) on the Progression of Primary Liver Cancer

Start date: January 2015
Phase: N/A
Study type: Interventional

Supplementation of BCAA found to reduce the risk of developing liver cancer, but the affect of BCAA on existing liver cancer is unknown. The participants (post curative intent surgery) will be supplemented with either BCAA/non-BCAA-enriched protein supplement. The intervantion will go on for 2 years or until a new liver tumor is found.