About this trial
Aim of the research is to assess frequency of MAFLD among patients with acute coronary syndromes (ACS).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
Patients refused to participate.
Patients with history of alcohol or drug abuse.
Patients have hepatitis C or hepatitis B infection.
Patients have primary or secondary hepatic malignancies
Trial population
Any Patient above the age of 18 years presented with acute coronary syndromes {myocardial infarction (MI), non-ST elevation myocardial infarction (NSTEMI), unstable angina} underwent coronary angiography within admission.
Trial design
Cohort
Cross-sectional
Treatments tested in this trial
fibroscan
DeviceFibroscan examination with controlled attenuation parameter"CAP" (Echosens FibroScan ® Compact 530) for evaluation of steatosis and its degree (by CAP score) and fibrosis stage by liver stiffness measurement(LSM)
Treatment groups
Trial outcomes
Primary outcomes
Assess frequency of MAFLD among patients with acute coronary syndromes (ACS).
patients with acute coronary syndrome will be evaluated if they have MAFLD and then we will know frequency of MAFLD among patients with acute coronary syndromes (ACS)
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: