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Application of one-stop internal and external crossbreeding in long term persistent atrial fibrillation and exploration of operative method

Application of one-stop internal and external crossbreeding in long term persistent atrial fibrillation and exploration of operative method

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000036625
Enrollment
Unknown
Registered
2020-08-24
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-09-21

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

Conditions

Atrial fibrillation

Interventions

Group A:Intervention of left atrium only: minimally invasive surgery performed left atrial ring pulmonary vein isolation + posterior wall box + left atrial appendage ligation, and then verification an
Group B:Left and right atrium intervention: left and right atrium isolation, left atrial ring pulmonary vein electrical isolation + posterior wall box + left atrial appendage ligation + right atrial s
Group C:Intervention of left atrium only: with the aid of three-dimensional mapping system, the left atrium was firstly mapped with matrix (voltage), and then ablation was guided according to the mapp
Group D:Left and right atrium intervention at the same time: with the assistance of three-dimensional mapping system of internal medicine, the matrix (voltage) mapping of left atrium and right atrium
Group E:Radiofrequency catheter ablation assisted by three-dimensional mapping system

Sponsors

The Ninth People's Hospital Affiliated to Medical School of Shanghai Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) The age was less than 75 years old and over 18 years old; 2) The duration of persistent AF was more than 1 week; 3) Long term persistent atrial fibrillation, atrial fibrillation time more than 1 year; 4) The diameter of left atrium was less than 60mm; 5) Cardiac function was nyhai-ii, and EF was more than 40%; 6) One month after stroke, the patient's muscle strength was above grade 4, and his mind was clear; 7) The researcher agreed to participate in the clinical trial and sign the informed consent, and agreed to conduct follow-up evaluation according to the requirements of the validation protocol.

Exclusion criteria

Exclusion criteria: 1) The atrial fibrillation caused by hyperthyroidism was before the hyperthyroidism was controlled; 2) Atrial fibrillation caused by rheumatic valvular disease; 3) Atrial fibrillation caused by congenital heart disease; 4) Patients with cor pulmonale and elevated pulmonary artery pressure had atrial fibrillation; 5) Patients with cardiomyopathy complicated with atrial fibrillation; 6) Acute or severe systemic infection; 7) Patients with previous open chest surgery such as CABG and valve replacement. 8) Patients with obvious bleeding tendency and hematological diseases; 9) Patients with aortic dissection or aortic aneurysm; 10) Patients with malignant tumor and end-stage disease; 11) Patients with any other conditions that the researchers consider unsuitable to participate in this trial; 12) From the perspective of medical ethics, researchers consider it necessary to terminate the study of patients.

Design outcomes

Primary

MeasureTime frame
Recurrence rate;

Countries

China

Contacts

Public ContactZhang Qingyong

The Ninth People's Hospital Affiliated to Medical School of Shanghai Jiaotong University

zhang_qingyong71@qq.com+86 18930172339

Outcome results

None listed

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