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Liver support treatment with plasma adsorption and exchange for hepatitis B liver failure

Studies a liver support treatment in adults with hepatitis B-related acute-on-chronic liver failure.

Plain-language title generated from the registry record
Registry title: Combination of DPMAS and Low Volume PE for Patients With HBV Related ACLF

Key facts

Where
Guangzhou, ChinaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Source: NCT04597164, who can take part

Where in China

  • Third Affiliated Hospital of Sun Yat-sen UniversityGuangzhou, ChinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Third Affiliated Hospital, Sun Yat-Sen University
Trial code
NCT04597164
Record updated
29 November 2024
Original description
This study is to investigate investigate the safety and efficacy of Double plasma molecular adsorption system with sequential low-dose plasma exchange in treating hepatitis B virus-related acute-on-chronic liver failure.Read full original descriptionShow less

Double Plasma Molecular Adsorption System With Sequential Low-Dose Plasma Exchange in Patients With Hepatitis B Virus-Related Acute-on-Chronic Liver Failure: A Prospective Cohort Study

This study is to investigate investigate the safety and efficacy of Double plasma molecular adsorption system with sequential low-dose plasma exchange in treating hepatitis B virus-related acute-on-chronic liver failure.

Inclusion: Clinical diagnosis of chronic hepatitis b virus infection (positive hepatitis b surface antigen or positive hepatitis b virus DNA > 0.5 year); Age from 18 to 65 years old; Clinical diagnosis of liver failure (serum total bilirubin level > 10 times upper limit of normal; prothrombin time activity < 40% and ≥20%, or prothrombin time international ratio ≤ 2.6 and > 1.5); Platelets > 50*10 E9/L.

Exclusion: Other important organ dysfunctions or transplantation; Other active liver diseases; Hepatocellular carcinoma or other malignancy; Human immunodeficiency virus infection or congenital immune deficiency diseases; Severe diabetes, autoimmune diseases; unstable infarction due to cardio-cerebrovascular events; Severe complications including severe infection, gastrointestinal bleeding, hepatic encephalopathy, hepatorenal syndrome; Pregnancy or lactation; Patients can not follow-up; Investigator considering inappropriate.

ClinicalTrials.gov NCT04597164