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Haemodynamics and Function of the Atria in Congenital Heart Disease by Cardiovascular Magnetic Resonance

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Completed

Conditions

Coarctation of the Aorta
Transposition of the Great Arteries
Tetralogy of Fallot

Study type

Observational

Funder types

Other

Identifiers

NCT02161471
Atrial function in CHD by CMR

Details and patient eligibility

About

The purpose of this study is to determine whether patients with repaired congenital heart disease show differences in size or function of their heart atria compared to normal controls and depending on the nature of their heart disease.

Full description

Atrial function is important for good ventricular filling and function. In patients with impaired cardiac function, atrial contraction is even more important. So far, the size and function of the atria have been assessed two-dimensionally by angiography and by echocardiography. However, these do not allow exact characterization of the volumetric changes of the atria during the cardiac cycle. Recently, cardiac magnetic resonance (CMR) has been used to assess size and function of the left atrium in adults. Little data are available about function and volume of the atria in children and the role of the atria in congenital heart disease (CHD).

The study will recruit patients with CHD (n=40) and normal controls (n=10). The patient group will be composed by patients suffering from the following conditions: coarctation of the aorta (n=10), tetralogy of Fallot (n=10), transposition of the great arteries after atrial switch (Senning procedure) (n=10), transposition of the great arteries after arterial switch operation (n=10).

The study consists of measurements of sizes and function of the right and the left atrium, respectively, by examining three-dimensional volume changes across the heart cycle, and of phase contrast measurements of blood flow across the valves of the heart.

Enrollment

22 patients

Sex

All

Ages

8+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Ability to perform repetitive breath holds of 10-15 seconds each
  • Written informed consent of the patients or their legal guardians

Exclusion criteria

  • Patients requiring general anaesthesia
  • Residual cardiac findings which might potentially influence the size and function of the atria

Trial design

22 participants in 2 patient groups

Tetralogy of Fallot
Description:
Patients after repair of tetralogy of Fallot
Normal
Description:
Normal controls

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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