Esophageal Temperature During PVI Using Q-DOT Micro
This study is looking at how two different methods of catheter ablation affect the temperature of your esophagus (the tube connecting your throat to your stomach) during a procedure for paroxysmal atrial fibrillation (a type of irregular heartbeat). Researchers will compare the QDOT Micro ablation catheter with the ST SF ablation catheter. The main goal is to see which method causes the smallest change in esophageal temperature during the ablation procedure. You may be able to join if you are 18 years or older and have been diagnosed with paroxysmal atrial fibrillation. The current recruitment status is unclear, and the study plans to enroll 30 participants.
- Study design
- This is a randomized controlled trial, meaning participants will be randomly assigned to one of two treatment groups. The study plans to enroll 30 participants.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- The primary endpoint, maximal change in esophageal temperature, is measured during the ablation procedure. Esophageal injury will be assessed by post-procedure capsule endoscopy.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Esophageal Temperature During PVI Using Q-DOT Micro
At a glance
Conditions
NCT06392932
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Cedars-Sinai Smidt Heart Institute
Los Angeles, Californiastudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Maximal change in esophageal temperature during posterior wall isolation.During ablation procedure.