PulseSelect™ PFA Global Registry
Recruiting now NCT06393920
Run by Medtronic Cardiac Ablation Solutions · for 18 and older · All sexes
What this study is about
The PulseSelect™ PFA Global Registry is a prospective, global, multi-center, observational post-approval study. Subjects will be treated with the PulseSelect™ PFA System and followed according to SOC.
Who can join (things the study team will check)
✅ You may be able to join if…
- Subject is ≥ 18 years of age or minimum age as required by local regulations.
- Subject has been diagnosed with atrial fibrillation (AF)
- Planned procedure using commercially available PulseSelect™ PFA System.
- Willing to comply with study requirements and give informed consent (defined as legally effective, documented confirmation of a subject's voluntary agreement to participate in this clinical study) or authorization per institution and geographical requirements.
🚫 You may not be able to join if…
- Subject is enrolled in a concurrent study that has not been approved for concurrent enrollment by the global study manager.
- Subject with exclusion criteria required by local law.
Where this trial is running
- Vancouver General Hospital, Vancouver, British Columbia, Canada
- McGill University Health Centre (MUHC), Montreal, Quebec, Canada
- Fuwai Hospital Chinese Academy of Medical Sciences, Beijing, China
- Fujian Provincial Hospital, Fuzhou, China
- The Second Affiliated Hospital of Harbin Medical University, Harbin, China
- Nanjing Drum Tower Hospital, Nanjing, China
- Ruijin Hospital Shanghai Jiao Tong University School of Medicine, Shanghai, China
- Fuwai Shenzhen Hospital Chinese Academy of Medical Sciences, Shenzhen, China
- The First Affiliated Hospital of Xinjiang Medical University, Ürümqi, China
- Wuhan Asia General Hospital, Wuhan, China
- The First Affiliated Hospital of Xiamen University, Xiamen, China
- Klinička Bolnica Dubrava, Zagreb, Croatia
+ 25 more sites.
Who to contact
Josman Suri · 7635050262 · josman.suri@medtronic.com
It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT06393920.
Verify everything on the official ClinicalTrials.gov record. Page updated July 2026.
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