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NCT06837441Completed

PerAF: AF Termination vs Prespecified Ablation

Atrial Fibrillation Termination Versus Prespecified Ablation for Persistent Atrial Fibrillation:A Pilot Study

Source: ClinicalTrials.gov · Last updated 20 Feb 2025

Brief summary (registry, in English)

The design of this study is an intervention, randomized, controlled study and contains two randomized groups:(1)AF-termination group;(2)Prespecified-ablation group.

Status (registry)
Completed
Study type
Interventional
Enrollment
195 (actual)
First submitted
16 Feb 2025
Start date
1 Jan 2023
Primary completion date
30 Jun 2023
Lead sponsor
Shanghai Chest Hospital
NCT number
NCT06837441

What you commit to

  • Study type: Interventional
  • Participants enrolled: 195
  • From 1 Jan 2023 to the primary completion date, 30 Jun 2023
  • 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.

Prior treatment

  • . The use of anticoagulant drugs is contraindicated;
  • .Prior left atrial ablation (surgical or catheter);

Other illness

  • .Uncontrolled congestive heart failure, EF \<35%;
  • . History of severe valve disease and/or prosthetic valve replacement;
  • . Myocardial infarction or stroke within 6 months;
  • . Severe congenital heart disease;
  • . Contrast agent allergy;
  • . Severe lung disease;
  • .Contraindications for cardiac catheterization;
  • .Have performed any cardiac surgery within 2 months;
  • .Life expectancy \< 12 months, including factors such as physical inability to tolerate ablation or unstable disease conditions.-

Other

  • . Left atrial diameter ≥60mm;
  • . Left atrial thrombus confirmed by preoperative esophageal ultrasound;
  • .Poor general health;

Who the study is looking for

  • aged between 18 and 80 years old;
  • Patients undergoing a first-time ablation procedure for PersAF, and in spontaneous AF at the beginning of the procedure;
  • Diagnosed as persistent AF according to the latest clinical guidelines,with atrial fibrillation lasting for at least one month;
  • Ineffective or intolerable to ≥1 anti-arrhythmia drug treatment;
  • Patients must be able and willing to provide written informed consent to participate in this study;
  • Patients must be willing and able to comply with all study follow- up requirements.

Age in the registry: 18 years to 80 years · Sex: All · Accepts 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
Shanghai Chest Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status

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