Effect of Diltiazem on Coronary Artery Ectasia

Sponsor
Ankara University (Other)
Overall Status
Completed
CT.gov ID
NCT02024919
Collaborator
(none)
60
1
2
35
1.7

Study Details

Study Description

Brief Summary

Coronary artery ectasia (CAE) has been defined as localized or diffuse dilatation of epicardial coronary arteries more than 1.5 fold of adjacent normal segments. Isolated CAE constitutes minor portion of the total CAE cases, with an incidence of 0.1% to 0.79% in which coronary artery stenosis or severe valvular heart diseases are not present. CAE represents not only an anatomical variant but also a clinical constellation of coronary artery disease (CAD) like association with myocardial ischemia and acute coronary syndromes. Patients with CAE without significant coronary narrowing may still present with angina pectoris, positive stress tests, or acute coronary syndromes. Impaired epicardial and microvascular perfusion were demonstrated in ectatic coronary arteries.

Myocardial blush grading (MBG) technique has been utilized in various conditions such as acute myocardial infarction, coronary artery ectasia, syndrome X and idiopathic dilated cardiomyopathy to evaluate myocardial perfusion.

There is still no consensus for management of CAE. Previously improvement of coronary flow has been demonstrated by mibefradil in patients with slow coronary flow. A new trial is needed to explore the effect of calcium channel blockers (CCB) in isolated CAE. Diltiazem improves myocardial perfusion by blocking calcium channels in coronary arteries. This agent has been widely used in coronary catheter labs to prevent and treat no-reflow.

The current study with prospective design was therefore set up to assess whether epicardial flow and tissue level perfusion would be improved by diltiazem in myocardial regions subtended by the ectatic coronary arteries among patients with isolated CAE.

Condition or Disease Intervention/Treatment Phase
  • Drug: intracoronary administration of diltiazem
  • Drug: intracoronary injection of 5 mL saline
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Diagnostic
Official Title:
Short Term Effect of Diltiazem on Myocardial Perfusion in Patients With Isolated Coronary Artery Ectasia- a Prospective Clinical Study
Study Start Date :
Jun 1, 2012
Actual Primary Completion Date :
May 1, 2015
Actual Study Completion Date :
May 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Diltiazem

intracoronary diltiazem 5 milligrams which is diluted with 5 mL of saline

Drug: intracoronary administration of diltiazem

Placebo Comparator: Saline

intracoronary saline 5 mL

Drug: intracoronary injection of 5 mL saline

Outcome Measures

Primary Outcome Measures

  1. Myocardial blush grade [within 3 minutes after intracoronary diltiazem administration]

    Myocardial blush grade which is a measure of myocardial perfusion will be analysed just after administration of intracoronary diltiazem.

  2. TIMI (Thrombolysis in myocardial infarction) flow grade [Within 3 minutes after intracoronary administration of diltiazem]

    TIMI (Thrombolysis in myocardial infarction) flow grade which is a measure of epicardial flow rate will be measured just after administration of intracoronary diltiazem

  3. TIMI (Thrombolysis in myocardial infarction) frame count [within 3 minutes after intracoronary administration of diltiazem]

    TIMI (Thrombolysis in myocardial infarction) frame count which is a measure of epicardial flow rate will be analysed just after administration of intracoronary diltiazem

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes

Inclusion Criteria: Patients with isolated coronary artery ectasia at least 1 major epicardial coronary artery

Exclusion Criteria:

Patients with known allergy to diltiazem acute coronary syndrome left ventricular systolic dysfunction significant valvular heart disease heart failure systolic blood pressure <90 mmHg heart rate <60 atrioventricular block (grade > I) severe liver or kidney failure significant coronary artery stenosis and patients on treatment with calcium channel blockers were excluded

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ankara University School Of Medicine, Department of Cardiology Ankara Turkey 06230

Sponsors and Collaborators

  • Ankara University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Özgür Ulaş Özcan, Dr, Ankara University
ClinicalTrials.gov Identifier:
NCT02024919
Other Study ID Numbers:
  • AnkaraU1
First Posted:
Dec 31, 2013
Last Update Posted:
May 6, 2015
Last Verified:
May 1, 2015
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 6, 2015