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Study for the correlation of plasma 12-HETE level with poor outcome in traumatic patients

Study for the correlation of plasma 12-HETE level with poor outcome in traumatic patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800018496
Enrollment
Unknown
Registered
2018-09-20
Start date
2018-10-01
Completion date
Unknown
Last updated
2018-09-24

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

Conditions

Trauma

Interventions

Trauma:no
non-Trauma:no

Sponsors

State Key Laboratory of Trauma, Burns, and Combined Injury, Department 1, Research Institute of Surgery, Daping Hospital, The Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 76 Years

Inclusion criteria

Inclusion criteria: Trauma group 1. Aged 18-76 years male and female; 2. ICU or traumatized hospitalized patients (patients admitted within 48 hours after trauma) 3. Signing of the letter of informed consent. Non-Trauma group including healthy people, patients with infections.

Exclusion criteria

Exclusion criteria: 1. patients with blood system diseases, abnormal lipid metabolism, and infectious diseases; 2. under 17 years of age; 3. pregnant and lactating women; 4. patients with mental disorders; 5. refuse to sign informed consent and refuse to provide information.

Design outcomes

Primary

MeasureTime frame
Plasma 12-HETE level;—

Secondary

MeasureTime frame
Incidence of sepsis after trauma;28-day mortality rate;Critical Illness score;28-day mortality rate;health related quality of life score;inflammatory response;Biochemical target;immune function;clinic outcome;—

Countries

China

Contacts

Public ContactHuaping Liang

Research Institute of Surgery, Daping Hospital, Army Military Medical University, Chongqing

13638356728@163.com+86 13638356728

Outcome results

None listed

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