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Early diagnosis andprognosis evaluation effects of the extracellular histones for ARDS induced by trauma

Early diagnosis andprognosis evaluation effects of the extracellular histones for ARDS induced by trauma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-15007217
Enrollment
Unknown
Registered
2015-09-28
Start date
2015-10-01
Completion date
Unknown
Last updated
2017-10-23

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

Conditions

Acute respiratory distress syndrome

Interventions

experimental group:Trauma Patients

Sponsors

Xiamen Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to No maximum

Inclusion criteria

Inclusion criteria: Trauma patients within 24 hours andhave signed an informed consent (ISS score>16); Including 30 cases of age-matched healthy adult volunteers as a control group.

Exclusion criteria

Exclusion criteria: Pregnant or lactating women; Younger than 18 years old; Patients with ARDS has been diagnosed when admitted to ICU; Patients with severe traumatic brain injury (GCS<8); Patients with chest trauma; Patients are expected 24 hours of death.

Design outcomes

Primary

MeasureTime frame
Histone;—

Countries

China

Contacts

Public ContactYe Huilong
sj_guo@163.com+86 18950027555

Outcome results

None listed

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