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NCT07487571Not yet recruiting

MPV as a Predictor for ACS in Patients With MASLD

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

Source: ClinicalTrials.gov · Last updated 6 May 2026

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
60 (estimated)
First submitted
17 Mar 2026
Start date
5 May 2026
Primary completion date
1 Nov 2026
Lead sponsor
Sohag University
NCT number
NCT07487571

What you commit to

  • Study type: Observational
  • Planned participants: 60
  • From 5 May 2026 to the primary completion date, 1 Nov 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients receiving antiplatelet or anticoagulant therapy prior to blood sampling.

Other illness

  • 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.

Lab values

  • Patients with known hematological disorders affecting platelet count or function.

Other

  • Pregnant or lactating females.

Who the study is looking for

  • 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.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sohag University Hospital
Coordinator of this site? Confirm its status
SohagEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.