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Completed

NCT Number: NCT03716934

CRyoAblation vs AntiaRrhythmic Drugs for Persistent Atrial Fibrillation Trial

This is a prospective, randomized, multicenter study comparing the relative efficacy and safety of cryoablation of PVs using the Arctic Front Advance® balloon catheter with antiarrhythmic therapy in patients with persistent AF.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Fundacion para Investigación Biomedica Hospital Clinico San Carlos

Madrid, 28040, Spain

About this study

The ablation of pulmonary veins is a very effective treatment for the treatment of paroxysmal atrial fibrillation. The benefit of the isolation of pulmonary veins in persistent atrial fibrillation seems to be minor and the level of scientific evidence available requires additional clinical trials to define the value of ablation in this type of patients.

The symptomatology of atrial fibrillation recurrences is variable among patients and among differens moments in the same patient. Pharmacological treatment and ablation have been used to reduce the symptomatology of atrial fibrillation recurrences and to increase the proportion of asymptomatic recurrences. Different forms of electrical monitoring of the heart rate are used to evaluate the effectiveness of an intervention. Frequents monitoring periods provide the information of the heart rate and the effect of any intervention.

The "Confirm RX heart monitor® (Abbott)" is a subcutaneous implantable device that provides continuous monitoring of the heart rate for more than 3 years without any effect on cardiac function. This implantable Holter automatically detects and saves atrial and ventricular arrhythmic episodes. The device can be analyzed in person or remotely, and can help to make decisions regarding anticoagulant and antiarrhythmic treatment of patients, while representing a powerful research tool for evaluate the effectiveness of different therapeutic options.

This is a prospective, randomized, multicenter study that compares the relative efficacy and safety of cryoablation of pulmonary veins using the Arctic Front Advance® balloon catheter with antiarrhythmic treatment in patients with persistent atrial fibrilation.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with recurrent persistent atrial fibrilation

Exclusion criteria

  • Patients with atrial fibrilation for more than one year at baseline
  • Atrial fibrilation prior ablation
  • Age> 75 years or <18 years
  • Hyperthyroidism
  • Hypertrophic cardiomyopathy
  • Severe valvular disease (stenosis or regurgitation)
  • Carriers of cardiac valves
  • Anteroposterior diameter of left atrium> 50 mm (left parasternal long axis)
  • Contraindications for anticoagulation
  • Left atrial thrombus
  • Anemia
  • Active infection
  • Pregnancy
  • Atrial fibrilation secondary to transient, avoidable or correctable causes (hyperthyroidism, pneumonia, pulmonary embolism, drugs, hydroelectrolytic alterations ...)
  • Life expectancy of less than 24 months
  • Participation in another non-purely observational study
  • Patients unable to understand treatment and / or study and / or providing adequate informed consent
  • Any condition, that in the opinion of the physician responsible for the patient, contraindicates any of the treatments of the study
  • Microalbuminemia

Treatment and study plan

Arctic Front Advance® balloon catheter

Device

Cryoablation of bidirectional block of all pulmonary veins

Antiarrhythmic drug

Drug

The drug will be chosen based on the preference of the researcher / responsible physician and current clinical practice guidelines.

Other names: Class I or III

Confirm RX heart monitor® (Abbott)

Device

Is a subcutaneous implantable device that provides continuous monitoring of the heart rate for more than 3 years without any effect on cardiac function

Primary outcomes

  1. Survival time with atrial fibrilation, auricular flutter or tachycardia

    Time frame: Up to 9 months.

    Survival time without atrial fibrilation, atrial flutter or atrial tachycardia of more than 2 minutes duration detected by Holter

  2. Presence of death or one major complications.

    Time frame: first month

    Presence of death or one of the following major complications: Stroke, systemic embolism, acute myocardial infarction, cardiac tamponade, need for transfusion, diaphragmatic paralysis lasting more than 24 hours or causing respiratory failure, atrioesophageal fistula, stenosis of pulmonary veins, Sustained (> 30 sec) or symptomatic ventricular tachycardia, Syncope secondary to bradyarrhythmias or tachyarrhythmias, Need for hospitalization due to cardiovascular causes or related to the study treatments, Any Serious Adverse Reaction or Serious Adverse Event related to the study treatments.

  3. Presence of death or one major complications.

    Time frame: fourth month

    Presence of death or one of the following major complications: Stroke, systemic embolism, acute myocardial infarction, cardiac tamponade, need for transfusion, diaphragmatic paralysis lasting more than 24 hours or causing respiratory failure, atrioesophageal fistula, stenosis of pulmonary veins, Sustained (> 30 sec) or symptomatic ventricular tachycardia, Syncope secondary to bradyarrhythmias or tachyarrhythmias, Need for hospitalization due to cardiovascular causes or related to the study treatments, Any Serious Adverse Reaction or Serious Adverse Event related to the study treatments.

  4. Presence of death or one major complications.

    Time frame: thirteen month

    Presence of death or one of the following major complications: Stroke, systemic embolism, acute myocardial infarction, cardiac tamponade, need for transfusion, diaphragmatic paralysis lasting more than 24 hours or causing respiratory failure, atrioesophageal fistula, stenosis of VP, Sustained (> 30 sec) or symptomatic ventricular tachycardia, Syncope secondary to bradyarrhythmias or tachyarrhythmias, Need for hospitalization due to cardiovascular causes or related to the study treatments, Any Serious Adverse Reaction or Serious Adverse Event related to the study treatments.

Secondary outcomes

  1. Percentage of patients without atrial fibrilation, flutter or tachycardia

    Time frame: first month

    Number of patients without atrial fibrilation, atrial flutter or atrial tachycardia of more than 2 minutes

  2. Percentage of patients without atrial fibrilation, flutter or tachycardia

    Time frame: fourth month

    Number of patients without atrial fibrilation, atrial flutter or atrial tachycardia of more than 2 minutes

  3. Percentage of patients without atrial fibrilation, flutter or tachycardia

    Time frame: thirteen month

    Number of patients without atrial fibrilation, atrial flutter or atrial tachycardia of more than 2 minutes

  4. Percentage of patient with cardioversion

    Time frame: first month

    Number of patients that need cardioversion

  5. Percentage of patient with cardioversion

    Time frame: fourth month

    Number of patients that need cardioversion

  6. Percentage of patient with cardioversion

    Time frame: thirteen month

    Number of patients that need cardioversion

  7. Percentage of patient with need to consult the emergency room or hospitalization due to cardiovascular events

    Time frame: first month

    Number of patients that need to consult the emergency room or hospitalization due to cardiovascular events

  8. Percentage of patient with need to consult the emergency room or hospitalization due to cardiovascular events

    Time frame: fourth month

    Number of patients that need to consult the emergency room or hospitalization due to cardiovascular events

  9. Percentage of patient with need to consult the emergency room or hospitalization due to cardiovascular events

    Time frame: thirteen month

    Number of patients that need to consult the emergency room or hospitalization due to cardiovascular events

  10. Percentage of patient with need a change or suspension of antiarrhythmic due to inefficiency

    Time frame: first month

    Number of patients that need a change or suspension of antiarrhythmic due to inefficiency

  11. Percentage of patient with need a change or suspension of antiarrhythmic due to inefficiency

    Time frame: fourth month

    Number of patients that need a change or suspension of antiarrhythmic due to inefficiency

  12. Percentage of patient with need a change or suspension of antiarrhythmic due to inefficiency

    Time frame: thirteen month

    Number of patients that need a change or suspension of antiarrhythmic due to inefficiency

  13. Percentage of patient with need for ablation or re-ablation not scheduled

    Time frame: first month

    Number of patients that need a ablation or re-ablation not scheduled

  14. Percentage of patient with need for ablation or re-ablation not scheduled

    Time frame: fourth month

    Number of patients that need a ablation or re-ablation not scheduled

  15. Percentage of patient with need for ablation or re-ablation not scheduled

    Time frame: thirteen month

    Number of patients that need a ablation or re-ablation not scheduled

Sponsors and collaborators

Lead sponsor

Hospital San Carlos, Madrid

Other

Registry information

Acronym: craft

Important dates

Study start
2018
Primary completion
2022
Study completion
2022
First posted
Oct 23, 2018
Registry last updated
Sep 15, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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