Coronary Artery Ectasia in Elective Coronary Angiography : Predictors, Outcomes and Management

Sponsor
Assiut University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03896321
Collaborator
(none)
60
1
4
18
3.3

Study Details

Study Description

Brief Summary

Coronary artery ectasia (CAE) is the diffuse dilatation of coronary artery. It is defined as a dilatation with a diameter of 1.5 times the adjacent normal coronary artery . Its prevalence ranges from 1.2%-4.9% with male to female ratio of 3:1 .

Coronary ectasia likely represents an exaggerated form of expansive vascular remodelling (i.e. excessive expansive remodelling) in response to atherosclerotic plaque growth .

CAE is more common in males. Hypertension is a risk Factor. Interestingly, patients with DM have low incidence of CAE. This may be due to down regulation of MMP with negative remodelling in response to atherosclerosis . Smoking appears to be more common in patients with CAE than in those with coronary artery disease (CAD).

The angiographic classification for CAE (described by Markis et al.) categorizes the severity based on the extent of coronary arterial involvement: Type 1: Diffuse ectasia of 2-3 arteries; Type 2: Diffuse ectasia in one artery and localized in another; Type 3: Diffuse single arterial ectasia; Type 4: Localized or segmental ectasia .

Stable angina is the most common presentation in patients with CAE . Patients with CAE without stenosis had positive results during treadmill exercise tests. ST-elevation myocardial infarction (MI) , non-ST elevation MI can occur from altered blood flow by distal embolization or occlusion of ectatic segment with thrombus.

Medical management for CAE is a controversial area as there is lack of evidence based medicine, especially the role of antiplatelet versus anticoagulant agents. Aspirin was suggested in all patients because of coexistence of CAE with obstructive coronary lesions in the great majority of patients and the observed incidence of myocardial infarction, even in patients with isolated coronary ectasia .The role of dual anti platelet therapy has not been evaluated in prospective randomized studies. Based on the significant flow disturbances within the ectatic segments, chronic anticoagulation with warfarin as main therapy was suggested

Condition or Disease Intervention/Treatment Phase
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Treatment
Official Title:
Coronary Artery Ectasia in Elective Coronary Angiography : Predictors, Outcomes and Management
Anticipated Study Start Date :
Apr 1, 2019
Anticipated Primary Completion Date :
Apr 1, 2020
Anticipated Study Completion Date :
Oct 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Asprin

Patient will receive dual anti platelet asprin And clopidogrel

Drug: Antiplatelet Agents
effect of dual antiplatelet in management of coronary artery ectasia

Active Comparator: Clopidogrel

Patient will receive dual anti platelet asprin And clopidogrel

Drug: Antiplatelet Agents
effect of dual antiplatelet in management of coronary artery ectasia

Active Comparator: Warfarin

Patient will receive oral anticoagulation

Drug: Anticoagulants
effect of oral anticoagulants in management of coronary artery ectasia

Active Comparator: Novel oral anticoagulant

Patient will receive oral anticoagulation

Drug: Anticoagulants
effect of oral anticoagulants in management of coronary artery ectasia

Outcome Measures

Primary Outcome Measures

  1. Efficacy of dual antiplatelet therapy vs oral anticoagulants in patients with CAE - occurance of major adverse cardiovascular events [6 months]

    Efficacy endpoints defined as the occurance of major adverse cardiovascular events (MACE)

  2. safety of dual antiplatelet therapy vs oral anticoagulants in patients with CAE - occurance of major or minor bleeding [6 months]

    safety endpoints of occurance of major or minor bleeding

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Subjects with suspected CAD who are referred for elective coronary angiography
Exclusion Criteria:
  • Previous admission with an acute coronary event, previous PCI or CABG.

  • History of bleeding tendency or those with high bleeding risk according to the HAS-BLED bleeding risk score

Contacts and Locations

Locations

Site City State Country Postal Code
1 Martina Gamil Assiut Egypt 23123

Sponsors and Collaborators

  • Assiut University

Investigators

  • Study Director: Salwa R. Demitry, Professor, Assiut University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Martina Gamil Fathi, Principal Investigator, Assiut University
ClinicalTrials.gov Identifier:
NCT03896321
Other Study ID Numbers:
  • Coronary Artery Ectasia
First Posted:
Mar 29, 2019
Last Update Posted:
Mar 29, 2019
Last Verified:
Mar 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 29, 2019