Geographic Mismatch as A Predictor of Short-Term Major Adverse Cardiovascular Events Following Long Coronary Stent Implantation

NCT07890181 · tracked via the Priya Life Science Egypt tracker

Sponsor

Sohag University

Phase

Observational

Started

2026-09-01

Last updated

2026-10-22

Condition(s) studied

Geographic MismatchShort-TermMajor Adverse Cardiovascular EventsLong Coronary Stent Implantation

Investigational drug(s) / intervention(s)

Coronary Stent Implantation

Coronary Stent Implantation: Patients undergo percutaneous coronary intervention (PCI) with successful implantation of a drug-eluting stent (DES) measuring ≥38 mm in length

Study summary

This study aims to evaluate whether geographic mismatch is an independent predictor of short-term major adverse cardiovascular events following long coronary stent implantation.

Eligibility

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

Inclusion Criteria: * Age ≥18 years old. * Both sexes. * Patients undergo percutaneous coronary intervention (PCI) with successful implantation of a drug-eluting stent (DES) measuring ≥38 mm in length. * Successful stent deployment with discharge after PCI. Exclusion Criteria: * Bare-metal stent (BMS) implantation. * Cardiogenic shock at presentation. * In-stent restenosis lesions. * Previous stent implantation in the target coronary segment. * Life expectancy \<6 months due to non-cardiac causes. * Incomplete clinical or geographic data. * Patients lost to follow-up immediately after hospital discharge.

Primary outcome measure(s)

Incidence of Major Adverse Cardiovascular Events — 30 days post-percutaneous coronary intervention
Incidence of Major Adverse Cardiovascular Events (MACE) will be recorded within 30 days post-percutaneous coronary intervention (PCI).

Trial sites (1)

Facility	City	Region	Status
Sohag University	Sohag	Egypt	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07890181 on ClinicalTrials.gov ↗ ← All trials in Egypt