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Clinical Trials in the Netherlands / NCT06846502
Active, not recruiting Not applicable

High Power Short Duration Radiofrequency Ablation of Atrial Fibrillation Using the QDOT MICRO™ Catheter

NCT06846502 · tracked via the Priya Life Science Netherlands tracker
Phase
Not applicable
Started
2023-06-21
Last updated
2025-02-26

Condition(s) studied

Atrial Fibrillation (AF)

Investigational drug(s) / intervention(s)

Pulmonary vein isolation

Pulmonary vein isolation: Compared to conventional radiofrequency (RF) ablation, which is performed with a power set of 30-40 Watt for a duration of 20-30 seconds, ablation with higher power and shorter duration (vHPSD, 90W/4sec) may result in more continuous and more durable ablation lesions with a similar safety profile, while reducing procedure duration.

Study summary

Atrial fibrillation (AF) is the most common cardiac arrhythmia worldwide, characterized by rapid and disorganized atrial activation leading to an irregular heart rhythm. Pulmonary vein isolation (PVI) ablation is the gold standard for catheter ablation based therapy. However, recurrence of AF after PVI is common, often due to the inability to create durable ablation lesions surrounding the pulmonary veins (PV). Conventional radiofrequency (RF) ablation is typically performed with power set at 30-40 Watt for a duration of 20-30 seconds. Previous studies have shown that ablation with very higher power and shorter duration (vHPSD, 90W/4sec) may result in more continuous and more durable ablation lesions with a similar safety profile as compared to conventional ablation lesions. This new technique may consequently improve outcomes of RF ablation for AF. Moreover, HPSD ablation of AF may significantly reduce RF duration, which could lead to shorter anaesthesia, fluoroscopy and procedure duration.

Cardiac magnetic resonance imaging (CMR) enables studying cardiac volumes, function and atrial tissue characteristics. By applying this imaging strategy before ablation, and directly (\<72 hours) and later (3 months) after ablation, transient (edema) and persistent (fibrosis) effects of RF ablation in the left atrial wall and surrounding tissues may be visualized and quantified.

The Q-POWER study aims to assess the effects of VHPSD RF ablation on 1) procedural characteristics, 2) acute and long-term ablation lesion formation and collateral tissue damage as assessed by CMR and 3) clinical outcomes in AF patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * \>18 years of age * AF and eligible for index PVI according to current ESC guidelines Exclusion Criteria: * Unwilling or unable to give written informed consent * Prior left atrial ablation * Other left atrial arrhythmias including atrial flutters * Prior left atrial surgery * Severe mitral valve regurgitation * Contraindication for gadolinium-based contrast agents * Contraindications for CMR (including metallic implants, cochlear implants, cardiac devices, neurostimulation systems, claustrophobia) * Renal insufficiency (eGFR \< 30 ml/min)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Amsterdam UMC Amsterdam North Holland

More Amsterdam UMC, location VUmc trials in the Netherlands

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06846502 on ClinicalTrials.gov ↗ ← All trials in the Netherlands