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Exploratory Study of the Genomics of Sepsis Patients in Highland and Plain Areas

Exploratory Study of the Genomics of Sepsis Patients in Highland and Plain Areas

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500106362
Enrollment
Unknown
Registered
2025-07-22
Start date
2023-12-13
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Sepsis

Interventions

Plains Group?:None
Plateau group?:None

Sponsors

The First Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Plateau group one: 1) meet the diagnostic criteria for sepsis 3.0 developed by the Sociey of Critical Care Medicine (SCCM)/European Society of Critical Care Medicine (ESICM); 2) Age>= 18 years old, Han nationality, gender is not limited; 3) Diagnosis of sepsis within 48 hours of admission; 4) The long-term (time>3 years) of the patient's (subject's) place of residence is >= 3000m above sea level;5) Agree to take blood samples for relevant omics testing, and the patient and his family members sign the informed consent form; 2.Plateau Group two: 1) Age>= 18 years old, Han nationality, gender is not limited;2) sepsis or other chronic diseases were not diagnosed at the time of sampling; 3) Agree to take blood samples for relevant omics testing, and the patient and his family members sign the informed consent form. 3.Plains group one: 1)met the diagnostic criteria for sepsis 3.0 developed by the Sociey of Critical Care Medicine (SCCM)/European Society of Critical Care Medicine (ESICM); 2) Age>= 18 years old, Han nationality, gender is not limited; 3) Diagnosis of sepsis within 48 hours of admission; 4) The long-term (time>3 years) of the patient's (subject's) place of residence is = 18 years old, Han nationality, gender is not limited; 2) sepsis or other chronic diseases were not diagnosed at the time of sampling; 3) Agree to take blood samples for relevant omics testing, and the patient and his family members sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Age< 18 years old; 2) Hospitalization is less than 24 hours; 3) patients with shock with an unclear diagnosis; 4) pregnant and lactating women; 5) end-stage malignant tumor; 6) Inability to obtain informed consent or authorization;

Design outcomes

Secondary

MeasureTime frame
APACHEII score;APTT;Hb;TT;Total bilirubin;Na;Fib;Fasting blood glucose;weight;PT;RBC;IL-6;Abdominal ultrasound;MONO;CRP;Lymphocyte subsets;Thoracoabdominal CT;Prealbumin;AST;ALT;WBC;height;Regular electrocardiogram;BMI;Direct bilirubin;Urea nitrogen;SOFA score;NEU%;calcium;creatinine;Blood gas analysis;PLT;Indirect bilirubin;PCT;K;Triglycerides;cholesterol;NEU;Albumin;LYM;cl;

Countries

China

Contacts

Public ContactYin Changlin

The First Affiliated Hospital of Army Medical University

ycl0315@163.com+86 139 8315 5227

Outcome results

None listed

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