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Biomarkers of organ dysfunctions and prognosis in perioperative sepsis patients

Biomarkers of organ dysfunctions and prognosis in perioperative sepsis patients

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200058717
Enrollment
Unknown
Registered
2022-04-15
Start date
2021-01-01
Completion date
Unknown
Last updated
2024-01-14

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

Conditions

sepsis

Interventions

Case group:None
Control group:None

Sponsors

Zhongshan Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria of Sepsis group: 1. Volunteer to participate in this clinical trial and sign the informed consent; 2. Patients to be operated in emergency surgery; 3. Age = 18 years and = 80 years; 4. Conform to Sepsis 3.0 diagnostic criteria: maladjustment of body response to infection and organ dysfunction, i.e. infection+SOFA = 2 points. Inclusion criteria of control group: 1. Volunteer to participate in this clinical trial and sign the informed consent; 2. The surgery plans to perform non infectious and non tumor surgery, such as lumbar surgery, cholecystolithiasis surgery, inguinal hernia surgery, etc; 3. Age = 18 years and = 80 years.

Exclusion criteria

Exclusion criteria: 1.The patients refuse.

Design outcomes

Primary

MeasureTime frame
Death in the hospital;

Secondary

MeasureTime frame
Incidence of septic shock;Occurrence of multiple organ dysfunction;

Countries

China

Contacts

Public ContactLinghui Jiang

Zhongshan Hospital of Fudan University

jiang.linghui@zs-hospital.sh.cn+86 13764350216

Outcome results

None listed

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