Skip to content

Imaging Flow Cytometry-Based Multi-Dimensional Neutrophil Profiling for Early Diagnosis and Prognosis of Sepsis/ARDS

Imaging Flow Cytometry-Based Multi-Dimensional Neutrophil Profiling for Early Diagnosis and Prognosis of Sepsis/ARDS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500104527
Enrollment
Unknown
Registered
2025-06-18
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Sepsis

Interventions

Sepsis/ARDS Group:None
Non-Sepsis/ARDS Group:None
Healthy Control Group:None

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Sepsis/ARDS group (1) Confirmed diagnosis of sepsis (in line with Sepsis 3.0 criteria)/ARDS (in line with the 2023 global definition of ARDS) within 48 hours of ICU admission; (2) Signed informed consent. 2. Non-sepsis/ARDS group; (1) Patients with severe non-sepsis/ARDS who have at least one or more organ dysfunction. (2) Signed informed consent. 3. Healthy control group (1) Signed informed consent; (2) There was no obvious abnormality in the results of physical examination.

Exclusion criteria

Exclusion criteria: 1. Sepsis/ARDS group (1) Survival time and ICU stay time less than 48 hours; (2) Age< 18 years old; (3) people with diseases that can cause neutrophil changes (such as autoimmune diseases, hematologic diseases, radiotherapy and chemotherapy); (4) People with a history of organ transplantation (patients who need to take immunosuppressants for a long time); (5) pregnant women; (6) Those who are unwilling to sign the consent form 2. Non-sepsis/ARDS group (1) Survival time and ICU stay time less than 48 hours; (2) Age< 18 years old; (3) people with diseases that can cause neutrophil changes (such as infections, autoimmune diseases, hematologic diseases, radiotherapy and chemotherapy); (4) People with a history of organ transplantation (patients who need to take immunosuppressants for a long time); (5) pregnant women; (6) Those who are unwilling to sign the consent form. 3. Healthy control group (1) Age< 18 years old; (2) people with diseases that can cause neutrophil changes (such as infections, autoimmune diseases, hematologic diseases); (3) People with a history of organ transplantation (patients who need to take immunosuppressants for a long time); (4) Patients with chronic diseases such as hypertension, diabetes, coronary heart disease, etc., including patients with tumors; (5) Those who are unwilling to sign the consent form.

Design outcomes

Primary

MeasureTime frame
Neutrophil Functional Indicators;Acute Physiology and Chronic Health Evaluation II, APACHE?;Neutrophil Mechanical Indicators;Sequential Organ Failure Assessment, SOFA;Neutrophil Morphological Indicators;

Countries

China

Contacts

Public ContactSang Ling

The First Affiliated Hospital of Guangzhou Medical University

sonysang999@vip.163.com+86 18588829307

Outcome results

None listed

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