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RECRUITINGOBSERVATIONAL

Correlation Between PLA Levels and Disease Severity in Patients With Sepsis Cardiac Insufficiency

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Sepsis cardiac insufficiency is characterized by high morbidity and mortality. Studies have shown an association between elevated PLA levels in patients with sepsis and clinical outcomes of cardiac dysfunction. This study will explore the correlation between circulating PLA levels and organ dysfunction and disease severity in SIMD patients in the form of a cross-sectional study.

Who May Be Eligible (Plain English)

Who May Qualify: - Sepsis cardiac insufficiency group 1. From April 2024 to December 2026, in the first ICU area of Dongzhimen Hospital, Beijing University of Chinese Medicine, Hospitalized patients in Zone II; 2. consistent with the diagnosis of sepsis cardiac insufficiency; 3. Age ≥ 50 and ≤ 90 years old; 4. SOFA score≥ 2 points; 5. Within 24 hours of the diagnosis of cardiac insufficiency in sepsis; 6. The patient or his/her family members sign the willing to sign a consent form form. Healthy subjects <!-- --> 1. Aged ≥ 50 and ≤ 90 years old, permanent residents of Beijing community; 2. Good health (blood routine, liver and kidney function, blood lipids, blood coagulation, no obvious abnormalities, no diagnosis cardiac insufficiency, acute coronary syndrome, old myocardial infarction, or cardiomyopathy); 3. There is no history of long-term use of drugs that affect platelet function and coagulation function, and those who are willing to cooperate with the test Crowd; 4. The subject himself signed the willing to sign a consent form form. Who Should NOT Join This Trial: ...See full criteria on ClinicalTrials.gov Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Sepsis cardiac insufficiency group 1. From April 2024 to December 2026, in the first ICU area of Dongzhimen Hospital, Beijing University of Chinese Medicine, Hospitalized patients in Zone II; 2. consistent with the diagnosis of sepsis cardiac insufficiency; 3. Age ≥ 50 and ≤ 90 years old; 4. SOFA score≥ 2 points; 5. Within 24 hours of the diagnosis of cardiac insufficiency in sepsis; 6. The patient or his/her family members sign the informed consent form. Healthy subjects <!-- --> 1. Aged ≥ 50 and ≤ 90 years old, permanent residents of Beijing community; 2. Good health (blood routine, liver and kidney function, blood lipids, blood coagulation, no obvious abnormalities, no diagnosis cardiac insufficiency, acute coronary syndrome, old myocardial infarction, or cardiomyopathy); 3. There is no history of long-term use of drugs that affect platelet function and coagulation function, and those who are willing to cooperate with the test Crowd; 4. The subject himself signed the informed consent form. Exclusion Criteria: * 1\) Diagnosed with acute coronary syndrome, old myocardial infarction, and coronary heart disease revascularization of patients; (2) Cardiac insufficiency due to cardiomyopathy, such as hypertrophic cardiomyopathy, dilated cardiomyopathy, myocardial amyloidosis, diabetic cardiomyopathy, hypothyroidic cardiomyopathy, etc.; (3) Due to heart knots Cardiac insufficiency caused by structural abnormalities, arrhythmias, cor pulmonale, nephroheart syndrome, etc.; (4) Impact Survival of severe primary diseases, including: uncontrolled malignant tumors that have metastasized in multiple places and cannot be resected, and blood disease, novel coronavirus infection and HIV, etc.; (5) Liver and kidney dysfunction with a single SOFA score of ≥3 points in liver or kidney handicappers; (6) Those who have been continuously using immunosuppressants or organ transplantation in the past 6 months; (7) 7 consecutive days prior to enrollment Those who have used corticosteroids, converted to methylprednisolone dose≥ 20mg/day; (8) Pregnant and lactating women; (9) Take or Injection of drugs that affect platelet function and coagulation function; (10) Those who have participated in other clinical trials within 30 days.

Locations (1)

DongzhimenH,Beijing
Beijing, Beijing Municipality, China