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A multicenter study investigating an early-warning model for cytokine storm in severe trauma

A multicenter study investigating an early-warning model for cytokine storm in severe trauma

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500109710
Enrollment
Unknown
Registered
2025-09-24
Start date
2025-07-04
Completion date
Unknown
Last updated
2025-09-29

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

Conditions

Severe multiple trauma, Inflammatory cytokine storm,MODS

Interventions

Observation group:NA

Sponsors

Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Samples from patients with severe polytrauma, an Injury Severity Score (ISS) >15, and who received treatment within 24 hours of injury. 2.Aged >=18 years, both male and female are eligible.

Exclusion criteria

Exclusion criteria: 1.Patients with a definitive diagnosis of open injuries at extremely high risk of infection (beyond Gustilo Type IIIA), hollow viscus injuries, or severe traumatic brain injury (TBI with AIS >= 3). 2.Having a confirmed source of infection or suffering from infectious diseases; at high risk of infection. 3.Women who are pregnant or breastfeeding. 4.Females aged 18-50 who are confirmed to be pregnant upon testing. 5.Severe primary diseases that affect survival (such as inoperable tumors, hematologic diseases, acute exacerbation of cardiovascular and cerebrovascular diseases and respiratory diseases, HIV, etc.). 6.Use of immunosuppressive agents within the past 6 months (total cumulative dose of glucocorticoids, converted to methylprednisolone, =1500 mg, and/or use of cytotoxic drugs), or use of either of the above two categories of drugs within the past 7 days. 7.Patients with psychiatric disorders. 8.Participants who have taken part in other clinical trials within the past 30 days. 9.Individuals whom the investigator deems unable or unsuitable to complete the study. 10.Patients with residual serum sample volume < 0.5 mL.

Design outcomes

Primary

MeasureTime frame
Cytokines: IL-18, IP-10, MCP-1, Eotaxin, MCP-4, CXCL12, MIP-3a, IL-1RA, Cystatin C, MRP8/14;

Countries

China

Contacts

Public ContactTianbing Wang

Peking University People's Hospital

wangtianbing@pkuph.edu.cn+86 13901166277

Outcome results

None listed

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