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.
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…
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