Építés alatt – nem éles oldal
Belépés
Not yet taking people in EgyiptomNo phase

MPV as a Predictor for ACS in Patients With MASLD

Key facts

Where
Sohag, EgyiptomSee the site

Where in Egyiptom

  • Sohag University HospitalSohag, EgyiptomNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Sohag University
Trial code
NCT07487571
Record updated
2026. május 6.
Original description
The aim of this study is to evaluate mean platelet volume (MPV) as a predictor of acute coronary syndrome (ACS) in patients with metabolic dysfunction-associated steatotic liver disease (MASLD to evaluate mean platelet volume (MPV) as a predictor of acute coronary syndrome (ACS) in patients with metabolic dysfunction-associated steatotic liver disease (MASLD) in Sohag University Hospital.Read full original descriptionShow less

Mean Platelet Volume as a Predictor for Acute Coronary Syndrome in Patients With Metabolic Dysfunction-associated Steatotic Liver Disease

The aim of this study is to evaluate mean platelet volume (MPV) as a predictor of acute coronary syndrome (ACS) in patients with metabolic dysfunction-associated steatotic liver disease (MASLD to evaluate mean platelet volume (MPV) as a predictor of acute coronary syndrome (ACS) in patients with metabolic dysfunction-associated steatotic liver disease (MASLD) in Sohag University Hospital.

Inclusion: Adult patients aged ≥18 years; Confirmed diagnosis of metabolic dysfunction-associated steatotic liver disease (MASLD) based on clinical, laboratory, and imaging criteria); Patients diagnosed with acute coronary syndrome (unstable angina, NSTEMI, or STEMI) for Group I; MASLD patients without clinical or electrocardiographic evidence of acute coronary syndrome for Group II; Patients who provide informed consent to participate in the study.

Exclusion: Patients receiving antiplatelet or anticoagulant therapy prior to blood sampling; Patients with chronic liver diseases other than MASLD (e.g., viral hepatitis, autoimmune hepatitis, alcoholic liver disease); Patients with active infection, inflammatory diseases, or malignancy; Patients with chronic kidney disease or end-stage renal failure; Patients with known hematological disorders affecting platelet count or function; Pregnant or lactating females.

ClinicalTrials.gov NCT07487571