Under construction – not a live service
Sign in
Not yet taking people in EgyptNo phase

MPV as a Predictor for ACS in Patients With MASLD

Key facts

Where
Sohag, EgyptSee the site

Where in Egypt

  • Sohag University HospitalSohag, EgyptNo 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
6 May 2026
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