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CompletedNCT00489788Updated Dec 11, 2013

Predictors for Pulmonary Valve Replacement - Anatomic and Hemodynamic Using MRI

An observational study in Congenital Disorders, sponsored by Emory University. Completed. Open to participants aged 3 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2013-12-11.

Sponsored by Emory University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
101
Ages
3 Years to 30 Years
Sex
All
01

Study summary

Magnetic Resonance Imaging (MRI) is a non-invasive test that can look at the heart without using radiation. An MRI will allow the doctors to look at the heart in order to assess how well the ventricle is pumping, the amount of blood that it is pumping in addition to how much it is stretching. An engineer at Georgia Tech has developed a new way of looking at an MRI. It is believed that this new way of looking at an MRI may be better able to tell us when to replace the valve in these children. If this new process works, not only can we apply it now but we will be able to look at previously performed MRIs and gather more information about these children and their heart function in order to help these and other children in the future.

We are planning on enrolling 30 subjects in this study. Some of the subjects will be enrolled and have their MRI strictly for the purpose of this study. Some of the subjects will be already scheduled for a routine MRI of their heart and we will ask them if we can do extra images for the study while they are already here.

Read the detailed description

Cardiovascular disease remains a leading cause of morbidity and death in the Western World. Assessment of Myocardial function has proven to be a clinically relevant method for monitoring and evaluating outcomes of medical therapy and surgery for structural lesions or acquired disease.

Tetralogy of Fallot (TOF) is the most common form of cyanotic congenital heart disease with a prevalence of 0.26 to 0.8 per 1000 live births The current surgical approach favors primary repair in infancy. This decreases the necessity for palliative procedures and has a low operative mortality. Complete repair often results in pulmonary regurgitation (PR), which is generally well tolerated in infancy. Late complications may include ventricular dilatation, tricuspid regurgitation, diastolic and systolic dysfunction, arrhythmias and sudden cardiac death.

Pulmonary valve replacement (PVR) is required in approximately 20% of patients with repaired TOF and has a 1-4% peri-operative mortality. Thus, early intervention may reduce irreversible right ventricle injury; however no definitive tools are presently available for determining patients at risk.

Myocardial strain analysis has not been critically evaluated to determine its value for predicting RV failure. This study will investigate the practicality and accuracy of a novel mathematical method, developed by the investigators, for analysis of cardiac deformation recovery from dynamic Cardiovascular Magnetic Resonance Imaging (CMRI) sequences. The proposed method requires structural MRI data, offering several important advantages over existing methods. These include reduced requirements in imaging time and analysis effort, and the option to use a large database of prior structural MRI studies of TOF patients in retrospective research.

This three-dimensional method is mathematically based on nearly incompressible tissue deformations. The project proposes validation of technique, comparing its results with current 'gold standard' methods that presently use CMRI myocardial tagging and phase velocity mapping, as a pilot study for clinical validation of strain imaging in TOF patients. The method tracks movement of myocardial tissue throughout the cardiac cycle to compute strain associated with normal and a clinical disease state.

During the study we will customize the method and software for specific use with CMRI and TOF. We will test the method on normal controls and TOF patients pre and post pulmonary valve replacement.

02

Conditions studied

  • Congenital Disorders

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Keywords

  • MRI
  • Ventricular Strain
  • Pulmonary Valve Replacement
  • Post Tetralogy of Fallot
03

In context

Tetralogy of Fallot

93 studies on the registry are indexed under Tetralogy of Fallot; 26 are open to participants now.

This study's enrollment of 101 is below the median of 120 across 39 observational studies indexed under Tetralogy of Fallot.

Browse Tetralogy of Fallot studies →

Lead sponsor

Emory University is the lead sponsor of 1,386 studies on the registry; 236 are open to participants now.

Of its 229 completed or terminated interventional studies of FDA-regulated products, 174 (76%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
3 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Pediatrics and young adults aged 3-30 years following surgical repair of Tetralogy of Fallot. Also looking at normal control subjects.

Inclusion criteria

  • Thirty (30) patients diagnosed with Tetralogy of Fallot.
  • Ten (10) patients with previously repaired post-PVR.
  • Ten (10) normal control subjects.
  • Meet the eligibility criteria for MRI.
  • Age range: 3-30 years
  • Informed consent being obtained from the legal guardians and/or patients.

Exclusion criteria

Exclusion Criteria:

  • Outside target age range.
  • Contra-indications to MRI such as metallic implants
  • Acquired (non-congenital) heart disease
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
101 participants (actual)
Patient registry
No
06

Study locations

No study locations are listed for this record.

07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 11, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00489788
Lead sponsor
Emory University
Collaborators
Children's Healthcare of Atlanta
Responsible party
W. James Parks, MD (Principal Investigator, Emory University) — Principal investigator
First posted
Jun 21, 2007
Start date
Sep 2008
Completion
Mar 2009
Last update
Dec 11, 2013

Study contacts

W.James Parks, MD
principal investigator · Emory University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2013. You cannot join it, but the record below documents what was studied.

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