A single-center prospective cohort study based on portable ECG equipment for early detection of arrhythmia after congenital heart disease operation

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2000035976

Enrollment

Unknown

Registered

2020-08-21

Start date

2020-12-01

Completion date

Unknown

Last updated

2020-08-31

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

Conditions

Congenital heart disease

Interventions

case series:N/A

Eligibility

Sex/Gender

All

Age

No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1. Children who may be complicated with arrhythmia after cardiac surgery, including atrial septal defect, Bostam malformation, single ventricle, transposition of great arteries and other diseases; 2. Children who were followed up for 1~3 months after operation.

Exclusion criteria

Exclusion criteria: 1. Children undergoing antiarrhythmic treatment; 2. Children who may undergo surgery during the follow-up period; 3. Children with NYHA heart function grade IV.

Design outcomes

Primary

Measure	Time frame
ITQOL;endpoint event (death, heart failure, reoperation due to arrhythmia or arrhythmia requiring treatment);	—

Countries

China

Contacts

Public ContactZhu Fang

Shanghai Children's Medical Center

dr.zhufang@gmail.com+86 15800387325

Outcome results

None listed

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