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Robotic Magnetic Navigation-guided high efficiency radiofrequency ablation strategy for atrial fibrillation

Robotic Magnetic Navigation-guided high efficiency radiofrequency ablation strategy for atrial fibrillation

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093830
Enrollment
Unknown
Registered
2024-12-12
Start date
2023-05-14
Completion date
Unknown
Last updated
2024-12-16

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

Conditions

atrial fibrillation

Interventions

vHPSD group:high power, short duration ablation
CPCD group:Conventional power, conventional duration ablation

Sponsors

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Patients with paroxysmal atrial fibrillation occurring at least once within six months or persistent atrial fibrillation lasting less than one year; 2.the patient or his guardian was informed of the nature of the trial and agreed to participate in all the terms of the trial, voluntarily signed the informed consent approved by the ethics committee; 3. age >= 18 years old, <= 75 years old; 4.agreed to accept the postoperative treatment plan and follow-up requirements, and was able to complete the follow-up and follow-up inspection requirements; 5.Poor efficacy or intolerance after treatment with at least one antiarrhythmic drug (such as amiodarone, propafenone, sotalol, dronedarone, etc.); Or patients who have obvious symptoms, and are still willing to undergo ablation surgery without medication.

Exclusion criteria

Exclusion criteria: 1. Rheumatic heart disease or pulmonary vein stenosis or previous implantation of pulmonary vein stents; 2. heart failure patients with cardiac function grade IV (NYHA); 3. Patients with myocardial infarction within 90 days before operation; 4. Individuals with a history of cardiac or PCI surgery within 90 days prior to ablation; 5. patients with stroke or transient ischemic attack (TIA) within 120 days; 6. thrombus in left atrium (LA) or left atrial appendage (LAA) according to TTE; 7. reversible causes of atrial fibrillation, including but not limited to uncontrolled hyperthyroidism, severe obstructive sleep apnea, and acute alcohol poisoning; 8. Pregnant or lactating female patients, or patients with mental disorders; 9. echocardiographic measurement of left atrial anteroposterior diameter >= 50 mm;

Design outcomes

Primary

MeasureTime frame
Long term success rate post ablation;

Secondary

MeasureTime frame
Short term success rate post ablation;ablation related complications;ablation related parameters;AFEQT and SF-12 Score in 12 months follow up;Biochemical index and echocardiography parameters in;

Countries

China

Contacts

Public ContactQi Jin

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine

jinqi127@163.com+86 21 64370045

Outcome results

None listed

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