Skip to content

Additional Impact of Very High Power Short-Duration Ablation on Esophageal Injury After Catheter Ablation of Persistent Atrial Fibrillation: A Single-Center, Prospective, Single-Arm Clinical Study

Additional Impact of Very High Power Short-Duration Ablation on Esophageal Injury After Catheter Ablation of Persistent Atrial Fibrillation: A Single-Center, Prospective, Single-Arm Clinical Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098582
Enrollment
Unknown
Registered
2025-03-11
Start date
2024-10-14
Completion date
Unknown
Last updated
2025-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

persistent atrial fibrillation

Interventions

experimental group:The "QMODE+" ablation mode is used to perform a "modified BOX lesion technique"

Sponsors

Yan'an Hospital, Kunming
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) The subject voluntarily participates in the trial and signs the informed consent form. (2) Age>= 18 years and < 80 years. (3) Patients with persistent atrial fibrillation undergoing their first catheter ablation procedure. (4) Subjects able to communicate effectively with the investigators and comply with the trial requirements.

Exclusion criteria

Exclusion criteria: (1) History of prior cardiac surgery and/or AF ablation. (2) History of rheumatic valvular disease. (3) Ischemic stroke or transient ischemic attack (TIA) within the past 6 months. (4) Contraindications to anticoagulation therapy. (5) Inability to undergo or contraindications to esophageal endoscopy, such as acute esophageal perforation. (6) Left atrial diameter > 55 mm (as measured in the parasternal long-axis view on transthoracic echocardiography). (7) Patients unable to complete the procedure due to complications. (8) Pregnant or breastfeeding women, patients with severe epilepsy or mental disorders, and individuals with alcohol or drug dependency. (9) Subjects currently participating in other clinical trials involving drugs or devices. (10) Any abnormality or condition that the investigator deems should exclude the subject from enrollment in this study.

Design outcomes

Primary

MeasureTime frame
Newly developed esophageal ulcer.;

Secondary

MeasureTime frame
incidence of serious perioperative complications;

Countries

China

Contacts

Public ContactShaolong Li

Yan'an Hospital, Kunming

13700651472@126.com+86 137 0065 1472

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026