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Outcome analysis after surgical or interventional correction of an aortic coarctation in infants

Outcome analysis after surgical or interventional correction of an aortic coarctation in infants - CoA in infants

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00028157
Enrollment
150
Registered
2022-03-11
Start date
2022-02-27
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Q25.1

Interventions

Group 1: Interventional patients Therapy: Balloon angioplasty with or without stent placement Group 2: surgical patients Therapy: resection with (extended) end-to-end anastomosis

Sponsors

Päd. Kardiologie und Intensivmedizin, OE6730,Medizinische Hochschule Hannover
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0 Days to 12 Months

Inclusion criteria

Inclusion criteria: -Age <12 months old -The patients should have received both echos we plan to analyze and the their therapy at our institution.

Exclusion criteria

Exclusion criteria: Complex congenital heart defects such as: Atrial Septal Defect Atrioventricular Septal Defect Double-outlet Right Ventricle d-Transposition of the Great Arteries Ebstein Anomaly Hypoplastic Left Heart Syndrome Pulmonary Atresia Single Ventricle Tetralogy of Fallot Total Anomalous Pulmonary Venous Return Tricuspid Atresia Truncus Arteriosus Ventricular Septal Defect These defects would make the speckle tracking analysis impossible to perform. Furthermore they are often simultaniously surgically repaired, thus not allowing us to study isolated effects of the coarctation correction. -> Should we have enough* neonates (<30 days old) with isolated aortic coartcation we would like to mostly focus on them, since this is the most typical and most critical in terms of complications and clinical manifestation. * we defined enough as a number of patients that would allow us to also perforn statistical analysis on the collected data. After a power calculation we came up with a number of min.20 patients: at least 10 Patients per group.

Design outcomes

Primary

MeasureTime frame
longitudinal, radial and circumferential left-ventricular strain and longitudinal right-ventricular strain

Secondary

MeasureTime frame
advanced echocardiographic parameters such as: LVEF, FAC, different diameters and wall thicknesses and different velocities measured at different segments of the aorta etc.

Countries

Germany

Contacts

Public ContactKlea Hysko

Päd.Kardiologie &IntensivmedizinMHH

Klea.Hysko@stud.mh-hannover.de05115329512

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026