Beyond Platelet Indices, WBC-to-MPV Ratio in Myocardial Infarction With Non-Obstructive Coronary Arteries (MINOCA) Correlate With Short-Term Rather Than In-Hospital Outcomes
1 other identifier
observational
80
1 country
1
Brief Summary
This study aims to evaluate the role of platelet indices and the \[White blood cell (WBC) /mean platelet volume (MPV)\] ratio in correlation with angiographic profiles of patients diagnosed with myocardial infarction with non-obstructive coronary arteries (MINOCA) to assess their predictive value for short-term clinical outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 10, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 10, 2025
CompletedFirst Submitted
Initial submission to the registry
July 12, 2025
CompletedFirst Posted
Study publicly available on registry
July 22, 2025
CompletedMarch 13, 2026
March 1, 2026
6 months
July 12, 2025
March 11, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
White blood cell count to mean platelet volume ratio (WMR)
White blood cell count to mean platelet volume ratio (WMR) will be recorded.
Within 6 hours of symptom onset
Secondary Outcomes (1)
Incidence of major adverse cardiovascular events
1 month post-procedure
Study Arms (2)
Study group
Myocardial infarction with nonobstructive coronary arteries (MINOCA) patients
Control group
Healthy control individual.
Interventions
Coronary angiograms will be acquired digitally for quantification.
Upon retrieval of a version from http://www.syntaxscore.com, the anatomical SYNTAX score will be implemented to numerically evaluate the intricacy of coronary lesions.
Eligibility Criteria
This case-control study will be performed at Sohag University Hospitals after approval from the institutional ethical committee.
You may qualify if:
- Age ≥18 years old.
- Both sexes.
- Patients with acute myocardial infarction (AMI). Myocardial infarction with nonobstructive coronary arteries (MINOCA) is diagnosed if a patient fulfilled the AMI criteria in the absence of obstructive coronary arteries (type I: \<50% stenosis; or type II: no stenosis) as recommended by the recent American Heart Association statement that introduces an updated definition incorporating the 4th universal MI definition, which by agreement excludes Takotsubo syndrome and myocarditis from the eventual diagnosis of MINOCA.
You may not qualify if:
- Previous history of MI or coronary revascularization (PCI or bypass surgery) with acute/chronic infection.
- Autoimmune diseases.
- Systemic inflammatory disease.
- Patients on treatment therapy which critically affects inflammatory cell count.
- Patients with malignancy.
- Chronic kidney disease.
- Severe liver disease.
- Severe anemia.
- Fever (\>38°C).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sohag Universitylead
Study Sites (1)
Sohag University
Sohag, 82511, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer of Cardiovascular, Faculty of Medicine, Sohag University, Sohag, Egypt.
Study Record Dates
First Submitted
July 12, 2025
First Posted
July 22, 2025
Study Start
January 1, 2025
Primary Completion
July 10, 2025
Study Completion
July 10, 2025
Last Updated
March 13, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
- Time Frame
- After the end of study for one year.
- Access Criteria
- The data will be available upon a reasonable request from the corresponding author.
The data will be available upon a reasonable request from the corresponding author after the end of study for one year.