Actively Recruiting
Explore Plasma Biomarkers and Platelet Morphological Signatures for Predicting Prognosis in Patients With Extracorporeal CardioPulmonary Resuscitation Using Multi-omics and Platelet Morphology Analysis
Led by Central China Fuwai Hospital of Zhengzhou University · Updated on 2026-03-23
130
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
C
Central China Fuwai Hospital of Zhengzhou University
Lead Sponsor
U
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating plasma biomarkers and platelet morphology to better understand and predict outcomes in patients undergoing extracorporeal cardiopulmonary resuscitation (ECPR) for cardiac arrest. This observational study focuses on identifying protein and metabolic markers along with platelet changes that may help select cardiac arrest patients who could benefit most from ECPR and improve prognostic assessments. The study is led by Central China Fuwai Hospital of Zhengzhou University and addresses current limitations in objective biomarker use for ECPR eligibility and prognosis. The study observes cardiac arrest patients before and after receiving ECPR treatment, analyzing plasma proteomic and metabolomic profiles as well as platelet ultrastructural changes. Patients are categorized based on their recovery status after ECPR, including those who fully recover, those with organ dysfunction, and those who suffer brain death or death. There are no experimental treatments given as this is an observational study collecting data to find potential predictive markers. Participants will be monitored for up to 30 days after ECPR treatment, during which researchers will assess survival rates and neurological outcomes using measurements such as 30-day mortality, hospital survival, cerebral performance category scale, left ventricular ejection fraction, oxygenation ratio, and serum levels of bilirubin and creatinine. The study involves detailed blood sample analysis and clinical assessments to track the progression and outcomes following ECPR intervention.
CONDITIONS
Brief Title
Plasma Biomarkers and Platelet Morphology of Extracorporeal CardioPulmonary Resuscitation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 70 years old (can be relaxed if good organ function and neurological prognosis after evaluation)
- Witnessed cardiac arrest with bystander traditional CPR started within 5 minutes
- Reversible causes of cardiac arrest such as cardiogenic, pulmonary embolism, severe hypothermia, drug poisoning, trauma, or acute respiratory distress syndrome
- No restoration of spontaneous circulation or hemodynamic instability after 20 minutes of traditional CPR, or spontaneous circulation restored but heart rhythm not maintained
- Signed informed consent
You will not qualify if you...
- Infectious diseases including hepatitis B, hepatitis C, AIDS, syphilis
- Hematological diseases such as hematological malignancies, aplastic anemia, idiopathic thrombocytopenic purpura (ITP)
- Malignant tumors outside the hematological system
- Recent or massive plasma or platelet transfusions during hospitalization
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Within 30 days after ECPR
Participants provide blood samples for plasma biomarker and platelet morphology analysis after receiving ECPR treatment.
1 to 2 visits depending on clinical status
Duration - Up to 30 days after ECPR
Participants are observed for survival and organ function outcomes following ECPR treatment.
Follow-up visits as needed within 30 days
Trial Site Locations
Total: 1 location
1
Fuwai Central China Cardiovascular Hospital
Zhengzhou, Henan, China
Actively Recruiting
Research Team
J
Jianchao Li
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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