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The effect of atrial substrate homogenerization on maintaining sinus rhythm in the patients with persistent atrial fibrillation

The effect of atrial substrate homogenerization on maintaining sinus rhythm in the patients with persistent atrial fibrillation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-ICR-15007016
Enrollment
Unknown
Registered
2015-09-04
Start date
2015-09-07
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Atrial fibrillation

Interventions

One:CPVI+CTI+Substrate homogenerization in the LA
Two:CPVI+CTI

Sponsors

The First Affiliated Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients with symptomatic persistent AF; Persistent AF will be defined as a sustained episode lasting > 7 days and less than 3 years; AF refractory or intolerant to at least1 class I or III antiarrhythmic medication; Patients age is18-75 years; Males or females; Patients signed the written informed consent for the study.

Exclusion criteria

Exclusion criteria: Patients with thromboemboli or tumor in LAA or LA (TEE or MSCT); Patients with left atrial size >=50 mm (2D echocardiography, parasternal long-axis view); Patients with atrial fibrillation because of reversal reason; Patients with cardiac operation history; Patients with previous radiofrequency ablation; Patients are allergic to antiarrythmic medications, anticoagulation drugs, adenosine, or isoprenaline; Patients with severe lung disease; Patients with stent implantation because of myocardial infarction or coronary heart disease; Patients are going to accept cardiac transplantation in recent 12 months; Patients in the acute phase of ischemic stroke; Patients with PLT count less than 80*10^9/L, or with contraindications to systemic anticoagulation with heparin or coumadin or a direct thrombin inhibitor; Patients with severe structural cardiac disease (medium or severe mitral regurgitation, DCM, HCM, other severe valvular heart diseases); Patients with abnormal thyroid function; Patients with severe liver or renal dysfunction ( AST or ALT more than 3 fold of upper limit value; the SCr >3.5mg/dl or Ccr < 30 ml/min); Patients who are in the period of pregnant; Patients with psychosis; Patients with life expectancy < 24 months.

Design outcomes

Primary

MeasureTime frame
SR at 0.5, 1, 2 years after ablation respectively;cardiac tamponade;

Countries

China

Contacts

Public ContactFengxiang Zhang
njzfx6@163.com+86 18136655088

Outcome results

None listed

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