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NCT06183619Active, not recruiting

Superior Vena Cava Isolation Plus Pulmonary Vein Isolation for Paroxysmal Atrial Fibrillation

Superior Vena Cava Isolation Plus Pulmonary Vein Isolation for Paroxysmal Atrial: a Multi-center Retrospective Study

Source: ClinicalTrials.gov · Last updated 14 Feb 2025

Brief summary (registry, in English)

Pulmonary vein isolation (PVI) for paroxysmal atrial fibrillation (PAF) has limited success. The superior vena cava (SVC) has been identified as one of the most common non-pulmonary vein triggers for PAF. It is estimated that SVC isolation (SVCI) could improve the clinical results of patients with PAF. However, results from previous studies about SVCI remain controversial. Safety concerns for SVCI may outweigh its benefits and lead to inadequate ablation. To address this issue, the introduction of a quantitative ablation index (AI) for SVCI may provide a solution. Therefore, the investigators sought to initiate a retrospective, multi-center study, to explore the efficacy and safety of quantitative SVCI in addition to PVI in PAF.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
400 (estimated)
First submitted
14 Dec 2023
Start date
1 Feb 2024
Primary completion date
30 Dec 2024
Lead sponsor
Chinese Academy of Medical Sciences, Fuwai Hospital
NCT number
NCT06183619

What you commit to

  • Study type: Observational
  • Planned participants: 400
  • From 1 Feb 2024 to the primary completion date, 30 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of any type of catheter ablation for cardiac arrhythmias.

Other

  • Sinus node dysfunction that requires permanent pacemaker implantation.

Who the study is looking for

  • Symptomatic paroxysmal AF that are unresponsive to antiarrhythmic drugs (one or more than one).
  • Willing to undergo catheter ablation for AF.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chinese Academy of Medical Science, Fuwai hospital
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.