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To explore the timing and efficacy of CVVHDF in the treatment of cytokine storm in sepsis of abdominal infection

To explore the timing and efficacy of CVVHDF in the treatment of cytokine storm in sepsis of abdominal infection

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053104
Enrollment
Unknown
Registered
2021-11-10
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-09-06

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

Conditions

Sepsis

Interventions

Experimental group:CVVHDF was administered on the basis of the Chinese Guidelines for the Emergency Treatment of Sepsis/septic shock (2018)
Control group:According to the Chinese Guidelines for emergency management of sepsis/septic shock (2018)

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18 to 75 years; 2.Patients diagnosed with sepsis (meeting the diagnostic criteria defined by Sepsis3.0: infection + organ dysfunction (SOFA score >=2)); 3.Meet cytokine storm criteria; 4.Informed consent signed by the patient or legal guardian.

Exclusion criteria

Exclusion criteria: 1.Pregnant or lactation patients; 2.HIV infection and other known immune deficiency patients (use of immunosuppressive drugs, cachexia or end-stage tumors, etc.) and patients with immune diseases such as systemic lupus erythematosus and rheumatoid disease; 3.Patients with existing chronic kidney disease requiring alternative treatment; 4.Patients who are participating in other clinical studies before screening; 5.Combined with uncontrollable bleeding or combined with blood transfusion reaction; 6.Other conditions that the researchers considered inappropriate for inclusion, such as: terminal state of chronic disease, no cure or survival possibility of discharge; Assess patients whose condition requires blood purification as a treatment.

Design outcomes

Primary

MeasureTime frame
Clinical index;Incidence of secondary organ failure;Days in intensive care;Use of vasoactive agents in intensive care units;Duration of mechanical ventilation during intensive care;Sequential organ failure score;

Secondary

MeasureTime frame
28-day survival rate;

Countries

China

Contacts

Public ContactTang Zhanhong

The First Affiliated Hospital of Guangxi Medical University

tangzhanhong139@sina.com+86 13978816316

Outcome results

None listed

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