Atrial Fibrillation Clinical Trial
— CRYO-AFOfficial title:
Cryoballoon Versus Irrigated Radiofrequency Ablation in Patients With Paroxysmal Atrial Fibrillation: A Multi-center, Prospective, Randomized, Controlled Study
| Verified date | February 2017 |
| Source | Ruijin Hospital |
| Contact | Qi Jin |
| jinqi127[@]163.com | |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
It's a multi-center, prospective, randomized, controlled clinical trial of cryoballoon versus radiofrequency ablation for paroxysmal atrial fibrillation.
| Status | Recruiting |
| Enrollment | 600 |
| Est. completion date | December 2020 |
| Est. primary completion date | June 2020 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 75 Years |
| Eligibility |
Inclusion Criteria: - ECG recording of atrial fibrillation - first time of ablation - refractory to at least one anti-arrhythmia drug - sign informed consent for participation in the study Exclusion Criteria: - had ablation before - serious heart failure - left atrial diameter>55mm - Myocardial infarction, heart surgery or coronary intervention in 3 months before the ablation - Stroke in 6 months before the ablation - Endocardial thrombosis |
| Country | Name | City | State |
|---|---|---|---|
| China | Shanghai Rui-Jin Hospital, Shanghai JiaoTong University School of Medicine | Shanghai | Shanghai |
| Lead Sponsor | Collaborator |
|---|---|
| Ruijin Hospital |
China,
Andrade JG, Khairy P, Macle L, Packer DL, Lehmann JW, Holcomb RG, Ruskin JN, Dubuc M. Incidence and significance of early recurrences of atrial fibrillation after cryoballoon ablation: insights from the multicenter Sustained Treatment of Paroxysmal Atrial — View Citation
Kuck KH, Brugada J, Fürnkranz A, Metzner A, Ouyang F, Chun KR, Elvan A, Arentz T, Bestehorn K, Pocock SJ, Albenque JP, Tondo C; FIRE AND ICE Investigators.. Cryoballoon or Radiofrequency Ablation for Paroxysmal Atrial Fibrillation. N Engl J Med. 2016 Jun — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Efficacy endpoint (time to first documented clinical recurrence after blanking period) | the time to first documented clinical recurrence after blanking period (month) | one year | |
| Primary | Safety endpoint (Any procedure-related complications) | Any procedure-related complications | one year | |
| Secondary | Procedure time (min) | skin to skin | one year | |
| Secondary | Left atrial time (min) | one year | ||
| Secondary | X-ray time (min) | one year | ||
| Secondary | time to first time cardiovascular hospitalization (month) | one year | ||
| Secondary | QoL changes at 12 months (Units on a Scale) | one year |
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