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Study of Coronary Artery Disease by Two Types of Angiography
This study is currently recruiting participants.
Verified by VA Connecticut Healthcare System, January 2006
Sponsored by: VA Connecticut Healthcare System
Information provided by: VA Connecticut Healthcare System
ClinicalTrials.gov Identifier: NCT00273819
  Purpose

The purpose of this study is to test the ability of a new X-ray technique called CT angiography to identify significant narrowing of the coronary arteries compared to traditional coronary angiogram.


Condition Intervention
Congestive Heart Failure
Procedure: CT angiography

MedlinePlus related topics: Coronary Artery Disease Heart Failure
U.S. FDA Resources
Study Type: Interventional
Study Design: Diagnostic, Non-Randomized, Single Blind, Historical Control, Single Group Assignment, Safety/Efficacy Study
Official Title: Non-Invasive Detection of Revascularizable Cardiomyopathy

Further study details as provided by VA Connecticut Healthcare System:

Primary Outcome Measures:
  • Detection of coronary disease by CT angiography

Secondary Outcome Measures:
  • Disease meets latest ACC/AHA guidelines for CABG

Estimated Enrollment: 30
Study Start Date: October 2005
Detailed Description:

Objective:

In patients with newly diagnosed cardiomyopathy it is the standard of care to perform coronary angiography. This procedure can separate ischemic from non-ischemic cardiomyopathy and identifies patients who may be eligible for revascularization as a therapeutic modality. With the advent of multidectector row-computed tomography technology, it is becoming possible to non-invasively identify significant atherosclerotic stenoses with acceptable sensitivity and specificity. The goal of this study is to compare non-invasive computed tomography (CT) angiography with traditional coronary angiography to identify proximal, and hence revascularizable, coronary artery disease in patients with cardiomyopathy. Revascularizable is defined a 3 vessel proximal disease, left main disease, or left main equivalent disease (ostial left anterior descending and ostial left circumflex).

Research Design:

This study is prospective, interventional, single site with the interpreting radiologists blinded to the results from previous angiography.

Methods:

Subjects will be patients with cardiomyopathy, defined as an ejection fraction less than 40%. Exclusion criteria include known allergy to contrast medium, previous anaphylaxis, and renal insufficiency (serum creatinine greater than 1.5). We would like to enroll 30 patients. After giving informed consent, all eligible patients will undergo CT angiography, performed using new multi-slice technology. The results of previously obtained transthoracic echocardiography and standard coronary angiography will be reviewed. Following CT angiography all patients will have a repeat measurement of serum creatinine to screen for contrast induced nephropathy. Results of the CT angiography will be analyzed to determine sensitivity and specificity for identifying revascularizable coronary artery disease, compared to coronary angiography as the gold standard.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Congestive heart failure with EF<40%
  • Age> 18 years

Exclusion Criteria:

  • Contrast allergy
  • Renal insufficiency
  • Inability or unwillingness to sign a consent
  • Diabetes Mellitus
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00273819

Contacts
Contact: Aseem Vashist, M.D. 2039325711 ext 2649 aseem.vashist@va.gov
Contact: Mehran Sadeghi, M.D. 2039325711 ext 3398 mehran.sadeghi@yale.edu

Locations
United States, Connecticut
VACT Healthcare System-Yale School of Medicine Recruiting
West HAven, Connecticut, United States, 06516
Contact: Fred Wright, M.D.     203-932-5711 ext 3968     fred.wright@va.gov    
Sub-Investigator: Brian Cambi, M.D.            
Sponsors and Collaborators
VA Connecticut Healthcare System
Investigators
Principal Investigator: Aseem Vashist, M.D. VACHS and Yale University School of Medicine
Principal Investigator: Mehran Sadeghi, M.D. VACHS and Yale University School of Medicine
  More Information

Study ID Numbers: AS0006, 00795
Study First Received: January 5, 2006
Last Updated: February 25, 2007
ClinicalTrials.gov Identifier: NCT00273819  
Health Authority: United States: Federal Government

Keywords provided by VA Connecticut Healthcare System:
Congestive heart failure, LV dysfunction

Study placed in the following topic categories:
Arterial Occlusive Diseases
Coronary Disease
Heart Failure
Heart Diseases
Myocardial Ischemia
Vascular Diseases
Arteriosclerosis
Ischemia
Cardiomyopathies
Coronary Artery Disease

Additional relevant MeSH terms:
Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 16, 2009