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A new optimized workflow of zero or near-zero fluoroscopy for catheter ablation of atrial fibrillation without the guidance of echocardiography

A new optimized workflow of zero or near-zero fluoroscopy for catheter ablation of atrial fibrillation without the guidance of echocardiography

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17014135
Enrollment
Unknown
Registered
2017-12-25
Start date
2016-11-20
Completion date
Unknown
Last updated
2018-01-08

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

Conditions

atrial fibrillation

Interventions

experimental group vs control group:optimmized workflow versus routine approach

Sponsors

Xin Hua Hospital affiliated to Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. With a history of paroxysmal Af(PAF) and PAF record within 6 months prior to ablation, confirming at least one of the following findings: AF lasting for =30 s recorded in Holter or 12-lead ECG; 2. No response to more than one antiarrhythmic drug, or unwilling to receive long-term drug treatment; 3. Can provide informed consent form expressing willingness to participate in the study and comply with follow-up tests and evaluation procedures; 4. Aged 18-80 years.

Exclusion criteria

Exclusion criteria: 1. With acute diseases, such as acute phase after myocardial infarction (within 3 months), within 3 months after acute heart failure or new cerebral infarction; 2. In the list of heart transplantation; 3. Expected survival less than 1 year; 4. With other hemorrhagic diseases and anticoagulant therapy is not allowed; 5. Thrombosis in left atrium; 6. Heart failure, NYHA III/IV or EF2 times upper limit of normal, CCr <50%); 9. Previous catheter radiofrequency ablation for AF or cardiac surgery; 10. Pregnant and lactating women, women who plan to become pregnant, or women of child bearing age not using reliable contraceptive measures.

Design outcomes

Primary

MeasureTime frame
success rate;complication rate;radiation exposure;

Countries

China

Contacts

Public ContactLi Yi-Gang

Xin Hua Hospital affiliated to Shanghai Jiao Tong University School of Medicine

drliyigang@outlook.com+86 13761318166

Outcome results

None listed

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