Correlation Between PLA Levels and Disease Severity in Patients With Sepsis Cardiac Insufficiency
Recruiting
Observational Study
Sepsis Cardiac Insufficiency
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
50 – 90
Sex
Any
Study type
Observational
Participants needed
30 (estimated)
Sponsor
Dongzhimen Hospital, Beijing · Other
Who this trial is looking for
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Answer a few quick questions to see if you may meet the eligibility requirements.
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.
Trial Locations
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Eligibility Criteria
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 …
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
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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.
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