Actively Recruiting
The Effects of Double Plasma Molecular Adsorption System in Acute on Chronic Liver Failure Patients
Led by Chulalongkorn University · Updated on 2025-12-29
40
Participants Needed
1
Research Sites
273 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Acute liver failure patients posed high mortality rate despite receiving standard therapy. The severity and mortality even higher in patients with underlying liver disease. Acute liver failure cause hyperinflammatory response in early stage and immunoparalysis in later stage. The surge of proinflammatory cytokines leads to multiorgan failure and more liver injury. Subsequent immunoparalysis may lead to lethal secondary infections. Liver support system had been used in acute and acute ontop chronic liver disease for last several decades. Double plasma molecular adsorption system (DPMAS) is one of the promising non-biological liver support system that have been extensively investigated in acute ontop chronic liver failure from hepatits B viral. DPMAS circuit consist of BS330 (bilirubin adsorber) and HA330 (Cytokines adsorber). Thus, DPMAS can also remove various cytokines. The effect of DPMAS on immune function in these patients has not been explored. Recent randomized controlled trial by Srisawat et al. demonstrated improvement of mHLA-DR in septic shock patients who received polymyxin B extracorporeal therapy compare to control arm. Since liver failure show change of immunological profile resemble to sepsis. Investigators proposed that removal of toxic liver toxins and lethal cytokines by DPMAS will improve immunological profiles in acute ontop chronic liver failure patients. Investigators plan to conduct a randomized controlled trial in acute ontop chronic liver failure patients who admitted to intensive care unit. Investigators plan to compare the immunomodulatory effects of DPMAS with standard treatments.
CONDITIONS
Official Title
The Effects of Double Plasma Molecular Adsorption System in Acute on Chronic Liver Failure Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 or more
- Diagnosis of acute on chronic liver failure by Asian Pacific Association for the Study of the Liver (APASL) criteria
- Admitted to intensive care unit
You will not qualify if you...
- Pregnancy
- Received steroid treatment
- Expected to die within 24 hours
- White blood cell count less than 500/mm3
- Allergy to Double Plasma Molecular Adsorption System (DPMAS)
- History of organ transplant
- Terminal illness with do not resuscitate order
AI-Screening
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Trial Site Locations
Total: 1 location
1
King Chulalongkorn Memorial Hospital
Bangkok, Thailand
Actively Recruiting
Research Team
P
Phatadon Sirivongrangson, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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