Skip to content

Short Term Warfarin Therapy for Radiofrequency Catheter Ablation of Atrial Fibrillation

Prospective Randomized Study of Incidence of Thromboembolic and Bleeding Events According to the Period of Warfarin Use Before and After Catheter Ablation of Paroxysmal Atrial Fibrillation in Low Risk Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01991951
Enrollment
520
Registered
2013-11-25
Start date
2013-07-31
Completion date
2017-07-31
Last updated
2013-11-25

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

Conditions

Atrial Fibrillation

Brief summary

We hypothesized that in patients with low CHADS-VASc score (2 or \< 2), there is no difference in thromboembolic or bleeding events between patients with short term warfarin therapy (2 weeks after catheter ablation) and conventional therapy (3 weeks before and 8 weeks after procedure).

Interventions

DRUGwarfarin

Sponsors

Korea University Anam Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with paroxysmal atrial fibrillation who underwent radiofrequency catheter ablation * Patients with CHADS-VASc score 2 or less than 2

Exclusion criteria

* Patients who do not consent to the study * Permanent or persistent atrial fibrillation * Patients who have underwent prior catheter ablation for atrial fibrillation * CHADS-VASc score more than 2 * History of stroke * LVEF \<40% * Significant liver or kidney dysfunction * History of major bleeding during warfarin therapy

Design outcomes

Primary

MeasureTime frame
Incidence of thromboembolic and bleeding events during 2 months2 months after the procedure

Countries

South Korea

Contacts

Primary ContactJaemin Shim, MD
jshim@kumc.or.kr82-10-6776-1195

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026