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The association between routine coagulation tests and clinical outcome in ICU traumatic patients—A cohort study

The association between routine coagulation tests and clinical outcome in ICU traumatic patients—A cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800019848
Enrollment
Unknown
Registered
2018-12-02
Start date
2018-12-13
Completion date
Unknown
Last updated
2018-12-04

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

Conditions

Sepsis

Interventions

Case series: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
17 Years to 76 Years

Inclusion criteria

Inclusion criteria: 1. ICU admission by trauma, traumatic infection or sepsis; 2. Aged between 18-76 years; 3. Hospital stay is more than 2 days; 4. Expected survival time > 7 days.

Exclusion criteria

Exclusion criteria: 1. ICU admission not by trauma, traumatic infection or sepsis; 2. Hospital stay is less than 2 days; 3. Missing a part of medical record.

Design outcomes

Primary

MeasureTime frame
Conventional coagulation function index;Incidence of sepsis;Mortality of sepsis;—

Secondary

MeasureTime frame
health related quality of life score;Critical Illness score;Biochemical target;—

Contacts

Public ContactHuaping Liang

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

13638356728@163.com+86 13638356728

Outcome results

None listed

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