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Application of heparin in patients undergoing radiofrequency ablation with a novel oral anticoagulant drug for atrial fibrillation

Application of heparin in patients undergoing radiofrequency ablation with a novel oral anticoagulant drug for atrial fibrillation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016491
Enrollment
Unknown
Registered
2018-06-04
Start date
2018-06-07
Completion date
Unknown
Last updated
2018-06-11

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

Conditions

Atrial Fibrillation

Interventions

New Oral Anticoagulant Group 1:Randomly administered initial heparin doses of 110 U/kg
Warfarin group:100 U/kg initial heparin dose
New Oral Anticoagulant Group 2:120 U/kg initial heparin dose
New Oral Anticoagulant Group 3:130 U/kg initial heparin dose

Sponsors

First Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years male and female; 2. First time radiofrequency ablation of atrial fibrillation; 3. Electrocardiogram, 24-hour dynamic electrocardiogram or ECG monitoring proved to be atrial fibrillation. 4. Patients receiving warfarin have INR between 2-3.

Exclusion criteria

Exclusion criteria: 1. Past cardiac surgery or intracardiac device implantation; 2. Left heart ejection fraction 55mm; 3. Moderate to severe valvular heart disease; 4. Reduced renal function (creatinine clearance 3); 5. Patients with acute coronary syndrome taking antiplatelet drugs; 6. Moderate to severe anemia (hemoglobin <90g/l); 7. Life expectancy less than 1 year.

Design outcomes

Primary

MeasureTime frame
Activated Clotting Time (ACT);

Countries

China

Contacts

Public ContactWang Na
1536261640@qq.com+86 18840855186

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026