Lipid Rich Necrotic Core Lesion Detected by Cardiac Magnetic Resonance Imaging (CMR)

NCT ID: NCT01284270

Last Updated: 2013-09-05

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-01-31

Brief Summary

The purpose of this study is to evaluate whether some features of plaques in coronary arteries predispose the heart muscle to injuries during angioplasty in patients with a narrowing in at least one of the arteries that may need a stent placed during a heart catheterization. Participants undergo a cardiovascular magnetic resonance imaging (MRI) study before the heart catheterization to look for scarring in the heart muscle. During the heart catheterization, participants undergo an intravascular ultrasound (IVUS) exam to look at the make-up of the plaques before the stent placement and the investigators will measure the pressures in the arteries to look at how severe the blockage is. Within 30 days after the heart catheterization, participants will have a second MRI done to look for any new scar in the heart muscle.

Conditions

Coronary Disease

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Blinding Strategy: NONE

Study Groups

All Patients

All patients undergo the same study procedures

Group Type: OTHER

Cardiac MRI

Intervention Type: OTHER

Cardiac MRI

Interventions

Cardiac MRI

Cardiac MRI

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Age 18 to 90 years
• Patients with known obstrucive coronary arterial disease for PCI in a native coronary artery
• Ability and willingness to consent and Authorization for use of personal health information (PHI)
• Ability and willingness to the required follow up procedures

Exclusion Criteria

• An acute myocardial infarction in the vascular territory of interest.
• History of percutaneous coronary intervention in the major epicardial vessel of interest
• Lesion characteristics that preclude IVUS
• The presence of delayed enhancement in the territory of the study vessel on baseline CMR
• Patients with current history of cardiomyopathy which is known to cause enhancement on CMR study
• Patients who are considered hemodynamically unstable based on clinical assessment by the physician
• Patients with Class IV congestive heart failure at time of enrollment
• Patients with poorly controlled hypertension with SBP >/= 210mmhg and/or DBP >/=140 hypertension unable to be treated, at time of enrollment
• GFR</=30 pre-procedure per institutional standards
• Patients with any known co-morbid conditions that is limiting their life expectancy to < 1year
• A known contraindication to Adenosine, including but not limited to:
• Moderate to severe hyperactive airway disease such as asthma and severe COPD
• Second or third degree AV block
• Known sinus node disease, such as sick sinus syndrome or symptomatic bradycardia
• Known hypersensitivity to Adenosine
• A known contraindication to MRI
• Electronically, magnetically, and mechanically activated implants
• Ferromagnetic or electronically operated active devices like automatic cardioverter defibrillators, and cardiac pacemakers
• Metallic splinters/fragments in sensitive tissues including the eye, brain, spinal cord etc…
• Ferromagnetic haemostatic clips in the central nervous system
• A known contraindication to Gadolinium
• Patients with history of allergic reactions to gadolinium based contrast
• Patients with glomerular filtration rate (GFR) </= 30ml/min
• Inability or unwillingness to consent and Authorization for use of PHI
• Patients who are unwilling or unable to follow up
• Known pregnancy

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Volcano Corporation

INDUSTRY

Sponsor Role: collaborator

GE Healthcare

INDUSTRY

Sponsor Role: collaborator

Siemens Medical Solutions

INDUSTRY

Sponsor Role: collaborator

Piedmont Healthcare

OTHER

Sponsor Role: lead

Responsible Party

Piedmont Heart Institute

Other Identifiers

Hawaii

Identifier Type: -

Identifier Source: org_study_id