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Epidemiological Study on Coagulation Dysfunction in ICUs in China

Epidemiological Study on Coagulation Dysfunction in ICUs in China

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125282
Enrollment
Unknown
Registered
2026-05-25
Start date
2025-01-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Coagulation disorders

Interventions

Observational group:None

Sponsors

The 908th Hospital of the Chinese PLA Logistics Support Force
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. At least 18 years old; 2. Patients admitted to the ICU for the first time; 3. At least one organ dysfunction present (SOFA score =2 for any single organ).

Exclusion criteria

Exclusion criteria: 1. Patients who are pregnant or breastfeeding; 2. Anyone with a known congenital bleeding disorder; 3. Those who have used anticoagulant or antiplatelet drugs within one month prior to admission.

Design outcomes

Primary

MeasureTime frame
Demographic and baseline characteristics including primary ICU diagnosis, sex, age, weight, and patient origin (emergency transfer, surgical ward transfer, medical ward transfer, operating room transfer, external hospital transfer);Past medical history including hypertension, diabetes mellitus, coronary heart disease, cerebral infarction, cerebral hemorrhage, etc.;Vital signs (worst values on the day of assessment: temperature, heart rate, respiratory rate, oxygen saturation, mean arterial pressure);Clinical scoring systems including APACHE II, SOFA, and Glasgow Coma Scale;Laboratory parameters (worst values on the day of assessment: complete blood count, blood biochemistry, coagulation profile, blood gas analysis);

Countries

China

Contacts

Public ContactSong Jingchun

The 908th Hospital of the Chinese PLA Logistics Support Force

songjingchun@126.com+86 189 7089 9900

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026