Low Fluoroscopy Afib Ablation Registry

Completed

Conditions studied: Atrial Fibrillation

In brief

Prospective data collection of patients undergoing Atrial Fibrillation Ablation.

Key facts

Study ID

NCT02830750

Run by

Stanford University

People needed

160

Starts

2016-04-01

Expected to finish

2018-04-01

Last updated by the study team

2018-04-26

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patient meets accepted AHA/ACC/HRS guideline indications for catheter ablation of paroxysmal or persistent AF
• First or subsequent ablation procedures may be included
• Age 18-75

You may not qualify if…

• Known venous malformations or implanted instrumentation (IVC filter)
• Known PV stenosis
• Unable to provide consent
• H/O mechanical mitral valve replacement (unable to rely on EA mapping only)
• Documented left atrial thrombus
• Prior ASD repair Pregnancy
• NYHA >=3
• EF less than 35%
• CHF within 90 daysRecent MI or coronary revascularization within 90 days
• NOTE: H/O implanted pacemaker or ICD with transvenous leads will NOT be an exclusion criteria, but we will track patients treated with pre-existing transvenous leads with the hypothesis that although fluoroscopy use will be higher in these patients compared to those without leads, but still lower than conventionally treated patients.
• Patients who are undergoing non- standard of care ablations ie, Cyro or FIRM ablations

Where it is running

• Beacon Medical Group — South Bend, Indiana, United States
• Brigham's Women's Hospital — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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