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Trial of Cardiac Magnetic Resonance Imaging (MRI) Versus Cardiac Catheterization Prior to Glenn Operation

Primary Purpose

Congenital Heart Defects

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Diagnostic cardiac MRI
Cardiac catheterization
Sponsored by
Boston Children's Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Congenital Heart Defects focused on measuring Superior cavo-pulmonary anastomosis, Glenn operation, Congenital heart defects, Cardiac magnetic resonance imaging

Eligibility Criteria

6 Weeks - 5 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Single ventricle heart disease patients presenting for Glenn operation Exclusion Criteria: Aortic arch obstruction Pulmonary vein stenoses Severe ventricular dysfunction Pulmonary hypertension

Sites / Locations

  • Childrens Hospital, Boston

Outcomes

Primary Outcome Measures

Toxicity profile for each group

Secondary Outcome Measures

Operative and post-operative outcomes
Missed diagnoses
Cost
Clinical Definition of successful Glenn operation

Full Information

First Posted
June 2, 2005
Last Updated
January 29, 2008
Sponsor
Boston Children's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00112424
Brief Title
Trial of Cardiac Magnetic Resonance Imaging (MRI) Versus Cardiac Catheterization Prior to Glenn Operation
Official Title
Clinical Trial of Cardiac Magnetic Resonance Imaging in Routine Evaluation Prior to Superior Cavo-Pulmonary Anastomosis
Study Type
Interventional

2. Study Status

Record Verification Date
January 2008
Overall Recruitment Status
Completed
Study Start Date
January 2004 (undefined)
Primary Completion Date
June 2006 (Actual)
Study Completion Date
January 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Boston Children's Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is a prospective, randomized study of patients with single ventricle heart disease who are to undergo superior cavo-pulmonary anastomosis, or "Glenn" operation. Such patients have historically undergone cardiac catheterization to ensure suitability for the procedure. Cardiac magnetic resonance imaging (cardiac MRI) is a newer technology that provides excellent anatomic and functional imaging of the heart. This study is designed to demonstrate our hypothesis that cardiac magnetic resonance imaging will provide comparable information to catheterization, with less side effects.
Detailed Description
This is a prospective, randomized study of patients with single ventricle congenital heart disease presenting for superior cavo-pulmonary anastomosis, or "Glenn" operation. Such patients in the past have routinely undergone pre-operative invasive cardiac catheterization to assess anatomic and hemodynamic suitability for this procedure. Recent retrospective reviews, including our own (J Thorac Cardiovasc Surg 2003: July;126(1):272-81) have suggested that such catheterization may not benefit many patients, and that non-invasive assessment may allow adequate evaluation while avoiding many (typically minor) complications seen with cardiac catheterization in this high risk group of infants. Cardiac MRI is a non-invasive imaging modality that can deliver superior anatomic information (such as vascular and intracardiac anatomy) as well as functional data (ventricular volumes and ejection fraction), and may be a safe alternative to catheterization in such patients. In this study, patients undergo screening echocardiogram prior to enrollment in the study to assess degree of risk for the operation (such as pulmonary vein obstruction, a clear risk factor for poor outcome) or for demonstrated need for catheterization intervention (such as aortic arch obstruction requiring balloon dilation); patients with low risk echocardiograms whose parents grant informed consent for the study are then randomized in a prospective fashion to cardiac MRI or cardiac catheterization. The findings of each study are then reviewed by the subject's cardiologist and cardiac surgeon; patients in whom further pre-operative information may cross over to another study if deemed necessary (such as catheterization in patients in whom an unsuspected finding is noted, or cardiac MRI in patients in whom further functional data may be desired). Patients are followed for details of the hospital stay (including hospital length of stay, complications, hospital charges) for the pre-operative testing, as well as operative and post-operative outcomes (new/missed diagnoses, hospital stay, operative and post-operative complications, achievement of a clinical definition of a "good" outcome from the Glenn operation).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Heart Defects
Keywords
Superior cavo-pulmonary anastomosis, Glenn operation, Congenital heart defects, Cardiac magnetic resonance imaging

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Diagnostic cardiac MRI
Other Intervention Name(s)
Cardiac Magnetic Resonance
Intervention Description
Routine cardiac MRI done under general anesthesia as pre-operative evaluation.
Intervention Type
Procedure
Intervention Name(s)
Cardiac catheterization
Other Intervention Name(s)
Cardiac cath.
Intervention Description
Routine cardiac catheterization prior to Glenn operation.
Primary Outcome Measure Information:
Title
Toxicity profile for each group
Time Frame
3 Months Post-Glenn operation
Secondary Outcome Measure Information:
Title
Operative and post-operative outcomes
Time Frame
30 days post-operation
Title
Missed diagnoses
Time Frame
3 months post-Glenn operation
Title
Cost
Time Frame
Pre-operative evaluation
Title
Clinical Definition of successful Glenn operation
Time Frame
3 months post-operatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Weeks
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Single ventricle heart disease patients presenting for Glenn operation Exclusion Criteria: Aortic arch obstruction Pulmonary vein stenoses Severe ventricular dysfunction Pulmonary hypertension
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David W. Brown, MD
Organizational Affiliation
Childrens Hospital Boston
Official's Role
Principal Investigator
Facility Information:
Facility Name
Childrens Hospital, Boston
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
12878965
Citation
Brown DW, Gauvreau K, Moran AM, Jenkins KJ, Perry SB, del Nido PJ, Colan SD. Clinical outcomes and utility of cardiac catheterization prior to superior cavopulmonary anastomosis. J Thorac Cardiovasc Surg. 2003 Jul;126(1):272-81. doi: 10.1016/s0022-5223(03)00054-0.
Results Reference
background
PubMed Identifier
15234431
Citation
Ro PS, Rychik J, Cohen MS, Mahle WT, Rome JJ. Diagnostic assessment before Fontan operation in patients with bidirectional cavopulmonary anastomosis: are noninvasive methods sufficient? J Am Coll Cardiol. 2004 Jul 7;44(1):184-7. doi: 10.1016/j.jacc.2004.02.058.
Results Reference
background

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Trial of Cardiac Magnetic Resonance Imaging (MRI) Versus Cardiac Catheterization Prior to Glenn Operation

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