Establishment of cardiac function evaluation method for congenital heart disease using high-speed Cine MRI imaging

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-jRCT1090220389

Enrollment

Registered

2018-09-27

Start date

2018-12-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Congenital Heart Disease

Interventions

Intervention type: Name of intervention: Dose form / Japanese Medical Device Nomenclature: Route of administration / Site of application: Dose per administration: Dosing frequency / Frequency of use:

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1)Congenital heart disease patients 2)Patients who are planning to cardiac MRI.

Exclusion criteria

Exclusion criteria: 1)Patients who cannot obtain consent from the person himself/herself or their parents 2)MRI contraindication (1)Claustrophobia (2)Patients with implanted metal in the body not compliant with MRI 3)Vital signs instability

Design outcomes

Primary

Measure	Time frame
Correlation of cardiac function obtained by the conventional and high-speed Cine MRI imaging method	—

Secondary

Measure	Time frame
Inter-observer agreement of detectability of right and left ventricular lumen	—

Countries

Japan

Contacts

Public ContactMakoto Orii

Iwate Medical University

kori931@gmail.com+81-19-651-5111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026