Evaluation of Remnant Cholesterol Levels and Monocyte-to-HDL-cholesterol Ratio As Predictors of Coronary Artery Disease Severity in Patients with Acute Coronary Syndrome
1 other identifier
observational
54
0 countries
N/A
Brief Summary
- 1.Evaluation of serum level of remnant cholesterol and monocyte/HDL ratio as predictors of severity of coronary artery disease in patients with acute coronary syndrome.
- 2.Evaluate predictive value of remnant cholesterol serum level and monocyte/HDL ratio to detect in-hospital worse clinical outcomes and 45 days major adverse cardiac events (MACE) after acute coronary syndrome.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Feb 2025
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
First Submitted
Initial submission to the registry
December 26, 2024
CompletedFirst Posted
Study publicly available on registry
January 3, 2025
CompletedStudy Start
First participant enrolled
February 8, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 8, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 8, 2026
CompletedFebruary 11, 2025
December 1, 2024
1 year
December 26, 2024
February 7, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Evaluation of serum level of remnant cholesterol and monocyte/HDL ratio as predictors of severity of coronary artery disease in patients with acute coronary syndrome.
Baseline
Secondary Outcomes (1)
Evaluate predictive value of remnant cholesterol serum level and monocyte/HDL ratio to detect in-hospital worse clinical outcomes and 45 days major adverse cardiac events (MACE) after acute coronary syndrome.
Baseline
Eligibility Criteria
Patients with acute coronary syndrome presented to ER of Assiut university hospital scheduled for primary PCI and able to provide informed consent
You may qualify if:
- Patients with acute coronary syndrome presented to ER of Assiut university hospital scheduled for primary PCI and able to provide informed consent.
You may not qualify if:
- Patients on previous statin therapy.
- Patients with severe renal dysfunction (creatinine clearance \<30 mL/min) or other contraindications to PCI.
- Patients with missed data or who couldn't be followed up
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (2)
Wadstrom BN, Wulff AB, Pedersen KM, Jensen GB, Nordestgaard BG. Elevated remnant cholesterol increases the risk of peripheral artery disease, myocardial infarction, and ischaemic stroke: a cohort-based study. Eur Heart J. 2022 Sep 7;43(34):3258-3269. doi: 10.1093/eurheartj/ehab705.
PMID: 34661640BACKGROUNDZegre-Hemsey JK, Asafu-Adjei J, Fernandez A, Brice J. Characteristics of Prehospital Electrocardiogram Use in North Carolina Using a Novel Linkage of Emergency Medical Services and Emergency Department Data. Prehosp Emerg Care. 2019 Nov-Dec;23(6):772-779. doi: 10.1080/10903127.2019.1597230. Epub 2019 Apr 17.
PMID: 30885071BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Isaac A Ghaly, Resident
Assiut University
- STUDY DIRECTOR
Hanan A Mahmoud, Lecturer
Assiut University
- STUDY DIRECTOR
Khaled A Mohamed, Lecturer
Assiut University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Resident doctor
Study Record Dates
First Submitted
December 26, 2024
First Posted
January 3, 2025
Study Start
February 8, 2025
Primary Completion
February 8, 2026
Study Completion
March 8, 2026
Last Updated
February 11, 2025
Record last verified: 2024-12