NCT06757777

Brief Summary

  1. 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. 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

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
54

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Feb 2025

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 26, 2024

Completed
8 days until next milestone

First Posted

Study publicly available on registry

January 3, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

February 8, 2025

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 8, 2026

Completed
28 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 8, 2026

Completed
Last Updated

February 11, 2025

Status Verified

December 1, 2024

Enrollment Period

1 year

First QC Date

December 26, 2024

Last Update Submit

February 7, 2025

Conditions

Keywords

AcsAcute coronary syndromeSTEMINON STEMIMonocyte/HDL Ratio

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

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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: 34661640BACKGROUND
  • Zegre-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

Acute Coronary SyndromeST Elevation Myocardial InfarctionNon-ST Elevated Myocardial Infarction

Condition Hierarchy (Ancestors)

Myocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesMyocardial InfarctionInfarctionIschemiaPathologic ProcessesPathological Conditions, Signs and SymptomsNecrosis

Study Officials

  • Isaac A Ghaly, Resident

    Assiut University

    PRINCIPAL INVESTIGATOR
  • Hanan A Mahmoud, Lecturer

    Assiut University

    STUDY DIRECTOR
  • Khaled A Mohamed, Lecturer

    Assiut University

    STUDY DIRECTOR

Central Study Contacts

Isaac A Ghaly, Resident

CONTACT

Hanan A Mahmoud, Lecturer

CONTACT

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