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Examination of Fibrillation Atria Using Magnetic Resonance Imaging and Endocardial High-density Mapping

Recruiting
Conditions
Atrial Fibrillation
Registration Number
NCT05539313
Lead Sponsor
Charles University, Czech Republic
Brief Summary

Cather ablation of non-paroxysmal atrial fibrillation is less effective compared to paroxysmal atrial fibrillation. Therefore, new techniques have been developed, such as high-density mapping to determine areas of focal and rotational activities. The aim is to assess the clinical efficacy of ablation focal and rotational activities, and to assess the relation between the areas of focal and rotational activities with fibrosis of both atria assessed using magnetic resonance.

Detailed Description

Pateints with non-paroxysmal atrial fibrillation will be enrolled. Before the procedure, cardiac magnetic resonance will be done to determine the extent and location of atrial fibrosis of both atria using dedicated software. The procedure itself will be done standardly, in alangosedation, from both femoral veins, using 10-pole catheter in the coronary sinus, intracardiac echocardiography, and two transseptal punctures by means of SL1 sheaths. Octarey mapping catheter (Biosense Webster, USA) wil be inserted in the left atrium, and during ongoing atrial fibrillation, a maping of left atrium will be done to locate the areas of focal and rotational activities. Afterthat, using Smart Touch ablation catheter (Biosense Webster, USA), pulmonary vein isolation will be done. When PVI is achieved, all areas of focal and rotational activities determined by high-density mapping will be performed. If sinus rhythm is achieved, the procedure is finished. If atrial fibrilaltion is organized to regular atrial, this regular tachacardia is mapped, ablated and the procedure is finished. If atrial fibrilaltion continues, mapping of the righ atrium using the same technique is done followed by catheter ablation of areas of focal and rotational activities. If atrial fibrillation is still present after all these ablation, electrical cardioversion will be done.

Patients will be discharged on following day. 5-day Holter recording will be done in 3, 6, and 12 months during standard out-patient controls.

The aim is to compare the findings of high-density mapping with findings on atrial MRI (relation between fibrosis on MRI and locations of rotational and focal activities). Furher aim is to assess the efficaccy of this kidn of ablation, i.e. the sinus rhythm maintenance in 3,6, and 12 months.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
50
Inclusion Criteria
  • non-paroxysmal atrial fibrillation
Exclusion Criteria
  • creatinine > 120 umol/l
  • claustrofobia
  • pregnancy
  • mechanical valve
  • significant valve disease
  • left ventricular dysfunction, EF less than 35%

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sinus rhythm maintenance1 year

The freedom from atrial fibrillation

MRI and high-density relation3 days

The relation between areas of location and rotational activities with atrial fibrosis location

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Cardiocenter, 3rd Medical School, Charles University and University Hospital Kralovske Vinohrady

🇨🇿

Prague, Czechia

Cardiocenter, 3rd Medical School, Charles University and University Hospital Kralovske Vinohrady
🇨🇿Prague, Czechia
Pavel Osmancik, MD, PhD
Contact
00420
pavel.osmancik@volny.cz
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