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The impact of HA380 hemoperfusion on organ dysfunction in patients with refractory septic shock

The impact of HA380 hemoperfusion on organ dysfunction in patients with refractory septic shock

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104367
Enrollment
Unknown
Registered
2025-06-16
Start date
2025-06-20
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

refractory septic shock

Interventions

HA380 hemoperfusion group:Administer HA380 hemoperfusion
Control group:None

Sponsors

The First People's Hospital of Lianyungang City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with septic shock =200 pg/ml; 3.Age between 18 and 80 years old (inclusive); 4.The patient or family member has a full understanding of the purpose and significance of this trial, voluntarily agrees to participate in this clinical trial, and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Pregnant or lactating women; 2.Patients with immunocompromise: ? Primary immunodeficiency diseases; ? Recipients of solid organ or bone marrow transplants; ? Patients receiving corticosteroid therapy at a daily dose>=20 mg prednisone or equivalent for >=14 days, or with a cumulative prednisone dose of 600 mg; ? Patients with malignant tumors undergoing chemotherapy; ? Patients receiving other immunosuppressive drugs (e.g., cyclosporine, cyclophosphamide, hydroxychloroquine, methotrexate); 3.Patients with coagulation disorders, active bleeding, or uncontrollable acute massive hemorrhage (within 24 hours); 4.Patients with malignant tumors and/or wasting diseases, those unable to undergo focus debridement (e.g., surgical patients unable to undergo operation), or those with low body weight (<35 kg); 5.Platelet count <20×10?/L; 6.Patients with a predicted mortality within 24 hours; 7.Patients who have participated in or are currently participating in any clinical study within the past month; 8.Other conditions deemed unsuitable for enrollment by the investigator.

Design outcomes

Primary

MeasureTime frame
The degree of dependence on vasoactive drugs in critically ill patients;

Secondary

MeasureTime frame
The degree of organ dysfunction or failure in critically ill patients;Blood interleukin-6 and procalcitonin;mortality rate;Mortality rate in the intensive care unit;In-hospital mortality rate;The duration of stay in the intensive care unit;Length of hospital stay ;ventilator-free days;

Countries

China

Contacts

Public ContactKang Xiuwen

The First People's Hospital of Lianyungang City

gnxy7iv@163.com+86 189 6132 2205

Outcome results

None listed

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