Efficacy and Safety of Cytokine Adsorption and Plasma Exchange in Patients With ACLF and Sepsis

Recruiting N/A Interventional Study
Acute-On-Chronic Liver Failure Sepsis
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 70
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
192 (estimated)
Sponsor
Third Affiliated Hospital, Sun Yat-Sen University · Other
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About This Trial
This study aims to evaluate the efficacy and safety of the double plasma cytokine adsorption system with sequential low-dose plasma exchange (DPCAS+LPE) in patients with acute-on-chronic liver failure (ACLF) complicated by sepsis. The focus is on assessing the impact of the cytokine adsorption column(CA280,Jafron Biomedical Co., Ltd., Zhuhai, China) on survival rates, inflammation markers, and org…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Age between 18 and 70 years with a background of chronic liver disease, regardless of the presence of cirrhosis. 2. Total bilirubin (TBIL) \> 12 mg/dL. 3. International normalized ratio (INR) ≥ 1.5. 4. Meeting the diagnostic criteria for sepsis: confirmed or suspected infecti…
Contacts

Liang Peng, Doctor

+8613533978874

pliang@mail.sysu.edu.cn

CONTACT

Wenxiong Xu, Doctor

+8613760783281

xuwenx@mail.sysu.edu.cn

CONTACT