Under construction – not a live service
Sign in
Taking people in ChinaNo phase

Comparing Catheter Ablation Approaches for Persistent Atrial Fibrillation

Compares heart rhythm ablation methods in adults with persistent atrial fibrillation.

Plain-language title generated from the registry record
Registry title: Optimized Ablation of the Posterior Wall in Persistent Atrial Fibrillation

Key facts

Where
Shanghai, ChinaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Source: NCT07122336, who can take part

Where in China

  • Shanghai Chest HospitalShanghai, ChinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Shanghai Chest Hospital
Trial code
NCT07122336
Record updated
14 August 2025
Original description
The design of this study is an intervention, randomized, controlled study and contains three randomized groups:(1)PVI group;(2)PVI+PWI group;(3)PVI+PWI+EGM group.Read full original descriptionShow less

Optimized Ablation of the Posterior Wall in Persistent Atrial Fibrillation

The design of this study is an intervention, randomized, controlled study and contains three randomized groups:(1)PVI group;(2)PVI+PWI group;(3)PVI+PWI+EGM group.

Inclusion: Age ≥18 years; First-time ablation for persistent atrial fibrillation (PsAF); Persistent AF definition: Sustained episodes lasting ≥7 days but ≤3 years (including episodes requiring pharmacologic or electrical cardioversion after ≥7 days); Symptomatic AF with intolerance to at least one antiarrhythmic drug (AAD); Documented PsAF episode: At least one recorded PsAF episode within the last 2 years prior to enrollment, confirmed by: ECG,Holter monitorin, Loop recorder, Telemetry, Transtelephonic monitoring (TTM),Implantable device; Ability and willingness to provide written informed consent; Compliance with all study follow-up requirements.

Exclusion: No prior attempt/pursuit of cardioversion or sinus rhythm maintenance; Advanced renal or hepatic failure; Severe valvular heart disease or cyanotic congenital heart disease; Long-standing persistent AF: Continuous AF duration >3 years; Paroxysmal AF: Episodes lasting <7 days (or requiring pharmacologic/electrical cardioversion <7 days); Contraindications to systemic anticoagulation; Pregnancy; Hypertrophic cardiomyopathy (HCM).

ClinicalTrials.gov NCT07122336