Status:

COMPLETED

Technical Development of Strain Rate Echocardiography

Lead Sponsor:

National Heart, Lung, and Blood Institute (NHLBI)

Conditions:

Echocardiography, Doppler

Eligibility:

All Genders

18+ years

Brief Summary

This study will examine heart function using two imaging techniques - echocardiography (ultrasound) and magnetic resonance imaging (MRI) - to evaluate newly developed software for echocardiograph mach...

Detailed Description

The purpose of this protocol is to study the reproducibility of strain rate (SR) echocardiography in normal volunteers and patients with cardiovascular disease. Tissue Doppler ultrasound is a technolo...

Eligibility Criteria

Inclusion

  • INCLUSION CRITERIA:
  • Adults older than 18 years will be recruited for the CAD group. Since regional wall motion abnormalities, coronary artery disease, and heart failure are rare in subjects under 21, we will limit this group to adults only.
  • Adults older than age 18 who have undergone surgical repair of Tetralogy of Fallot will be recruited. Normal controls will be age-matched to this group of patients.
  • Able to provide written informed consent.
  • EXCLUSION CRITERIA:
  • Patients with pulmonary artery shunts placed within the last 6 months are not eligible to undergo MRI scanning.
  • Pregnant or lactating (patients with uncertain pregnancy status will be required to have a screening urine or blood pregnancy test).
  • Chronic atrial fibrillation; frequent PVC's (more than 1 every 10 heart beats).
  • Cardiac pacemaker, defibrillator, or other metallic implant which would exclude subject from MRI examination (examples: central nervous system aneurysm clips, implanted neural stimulator, cochlear implant, ocular foreign body, insulin pump, metal shrapnel or bullet).
  • Inability to provide written informed consent.
  • Patients with hemoglobinopathies or renal disease with a creatinine clearance (CrCl) less than 20 ml/min will be excluded from MRI sequences involving administration of MRI contrast agents.

Exclusion

    Key Trial Info

    Start Date :

    January 8 2004

    Trial Type :

    OBSERVATIONAL

    End Date :

    October 17 2007

    Estimated Enrollment :

    125 Patients enrolled

    Trial Details

    Trial ID

    NCT00075920

    Start Date

    January 8 2004

    End Date

    October 17 2007

    Last Update

    July 2 2017

    Active Locations (1)

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    1

    National Institutes of Health Clinical Center, 9000 Rockville Pike

    Bethesda, Maryland, United States, 20892