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Arrhythmogenic Risk Assessment in Coronary Artery Ectasia Patients

Arrhythmogenic Risk Assessment in Coronary Artery Ectasia Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05106530
Enrollment
90
Registered
2021-11-03
Start date
2022-01-01
Completion date
2023-01-01
Last updated
2021-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Ectasia

Keywords

Coronary artery ectasia

Brief summary

The investigators thought to explore arrhythmias outcome - hidden arrhythmias, ECG features: Tp-Te interval and Tp-Te/QTc ratio, fQRS among patients with coronary artery ectasia as compared to normal coronary artery patients.

Detailed description

All patients will be subjected to: A. Full history taking: \- Including age, sex, history of DM, HTN, dyslipidemia and Body surface area. B. Holter monitoring for 24 hours: * Heart rate variability * Hidden arrhythmias * Hidden ischemia by monitoring ST segment changes C. Twelve lead ECG: * fQRS in baseline ECG * QT dispersion. * Tp-Te interval and Tp-Te/QTc ratio * Tp-Te dispersion

Interventions

DIAGNOSTIC_TESTHolter, ECG

Incidence of arrhythmias in Holter monitoring among coronary artery ectasia patients as compared to normal coronary artery patients.

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Subjects with suspected CAD who are referred for elective coronary angiography and/or interventions

Exclusion criteria

1. Patients with a history of cardiomyopathy and myocardial infarction (MI), left ventricular hypertrophy (LVH), pathological Q wave on ECG, typical left bundle block or right bundle block, incomplete right bundle block, or paced rhythm on ECG. 2. Patients with severe renal impairment 3. Post CABG patients 4. Patients of acute coronary syndrome

Design outcomes

Primary

MeasureTime frameDescription
Precence of arrhythmias in 24 hours Holter monitoring1 yearIncidence of arrhythmias in Holter monitoring among coronary artery ectasia patients as compared to normal coronary artery patients.

Secondary

MeasureTime frameDescription
• Heart rate variability in Holter monitoring1 yearHeart rate variability in Holter monitoring among coronary artery ectasia patients as compared to normal coronary artery patients.
• Silent ischemia as detected by Holter1 yearsPresence pf ischemia in Holter monitoring among coronary artery ectasia patients as compared to normal coronary artery patients.

Countries

Egypt

Contacts

Primary ContactMark M N Kamel, Resident
markkamel1994@yahoo.com+201274327737
Backup ContactHamdy Shams El Deen, Professor
hamdyshams@aun.edu.eg+201065601161

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026