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The Efficacy and Safety of Resin Adsorption Column-Based Adsorption Therapy in Reducing Inflammatory Response in Sepsis Patients

The Efficacy and Safety of Resin Adsorption Column-Based Adsorption Therapy in Reducing Inflammatory Response in Sepsis Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113779
Enrollment
Unknown
Registered
2025-12-03
Start date
2025-12-10
Completion date
Unknown
Last updated
2025-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sepsis

Interventions

Observation Group:Conventional treatment + adsorption therapy
Control Group:Conventional treatment

Sponsors

The First Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.In accordance with the Sepsis-3.0 definition and diagnostic criteria jointly released by the Society of Critical Care Medicine (SCCM) and the European Society of Intensive Care Medicine (ESICM) in 2016; 2.Sepsis diagnosis time =500 ng/L(pg/mL); 4.Age between 18 and 75 years old (inclusive), gender unrestricted; 5.The patient signs the informed consent form personally. If the patient is unconscious (e.g., due to coma, shock, or anesthesia) and unable to provide consent, their legal representative may sign the informed consent form on their behalf;

Exclusion criteria

Exclusion criteria: 1.Pregnant or breastfeeding women, or patients of childbearing potential unwilling/unable to use effective contraception; 2.Hypersensitivity to extracorporeal circulation materials, anticoagulants, or hemoperfusion agents, or a history of other severe allergies; 3.Patients with severe irreversible diseases, including terminal-stage malignancies; 4.Patients with immunodeficiency disorders, such as human immunodeficiency virus (HIV)/acquired immunodeficiency syndrome (AIDS); 5.Patients with severe acute liver failure (defined as prothrombin activity [PTA] 65 mmHg despite vasopressor support equivalent to >=1 µg·kg?¹·min?¹ of norepinephrine (dose conversion criteria refer to Appendix 1); 12.The investigator deems that participation in the trial poses significant risks to the patient's health or safety, may compromise efficacy evaluation, or presents other conditions unsuitable for inclusion in this study.

Design outcomes

Primary

MeasureTime frame
Changes in inflammatory cytokine levels (IL-6, CRP, PCT);

Secondary

MeasureTime frame
Other inflammation-related cytokines: IL-10, IL-1, TNF-a, IL-4, IL-8, IL-2, IL-35, HMGB-1, IFN-?;

Countries

China

Contacts

Public ContactQindong Shi

The First Affiliated Hospital of Xi'an Jiaotong University

shiqindong@163.com+86 29 85323215

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026