Arrhythmogenic Risk Assessment in Coronary Artery Ectasia Patients

NCT ID: NCT05106530

Last Updated: 2021-11-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

90 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-01-01

Study Completion Date

2023-01-01

Brief Summary

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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

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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

Conditions

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Coronary Artery Ectasia

Keywords

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Coronary artery ectasia

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

OTHER

Study Groups

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Coronary Artery Ectasia patients

Holter, ECG

Intervention Type DIAGNOSTIC_TEST

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

Normal coronary artery patients

Holter, ECG

Intervention Type DIAGNOSTIC_TEST

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

Interventions

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Holter, ECG

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

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Assiut University

OTHER

Sponsor Role lead

Responsible Party

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Mark Mohsen Nady Kamel

Resident at Cardiology Department

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Tarek Abd El Hameed, Assistant Professor

Role: PRINCIPAL_INVESTIGATOR

Assiut University

Locations

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Faculty of Medicine Assiut University

Asyut, , Egypt

Site Status RECRUITING

Countries

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Egypt

Central Contacts

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Mark M N Kamel, Resident

Role: CONTACT

Phone: +201274327737

Email: [email protected]

Hamdy Shams El Deen, Professor

Role: CONTACT

Phone: +201065601161

Email: [email protected]

Other Identifiers

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Arrhythmias in CAE patients

Identifier Type: -

Identifier Source: org_study_id