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Refralon in Patients With Recurrence Paroxysmal and Persistent Forms of Atrial Fibrillation Who Underwent Catheter Ablation

Primary Purpose

Atrium; Fibrillation, Atrium; Flutter

Status
Recruiting
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
Pharmacological cardioversion with Refralon
Sponsored by
National Medical Research Center for Cardiology, Ministry of Health of Russian Federation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrium; Fibrillation focused on measuring atrial fibrillation and flutter, paroxysmal and persistent atrial fibrillation and flutter, cardioversion AF, catheter radiofrequency ablation, Refralon, Niferidil, new antiarrhythmic drug, balloon cryoablation, reccurrence atrial fibrillation and flutter

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

2. Patients with paroxysmal or persistent forms of AF/AFL and early (less than 90 days) or late (more than 90 days) arrhythmia recurrence after catheter radiofrequency ablation or balloon cryoablation of pulmonary veins.

3. Indications for SR recovery. 4. Consent of the patient.

Exclusion Criteria:

  1. Arrhythmogenic effect of antiarrhythmic drugs III class in history;
  2. Chronic kidney disease with a decrease in glomerular filtration rate less than 30 ml / min / 1.73 m2;
  3. Chronic heart failure (functional class IV);
  4. Acute coronary syndrome;
  5. Bronchial asthma of an uncontrolled course and / or severe respiratory failure.
  6. The need for the use of drugs that increase the duration of the QT interval drugs without the possibility of withdrawal
  7. Atrioventricular blockade of 2-3 degrees (with the exception of patients with an implanted pacemaker);
  8. Dysfunction of the sinoatrial node (with the exception of patients with an implanted pacemaker);
  9. Bradysystolic atrial fibrillation (heart rate <50 beats/min);
  10. Duration of the QT interval >440 ms;
  11. Hemodynamic instability requiring emergency cardioversion;
  12. Contraindications to anticoagulant therapy;
  13. Thyrotoxicosis or decompensated hypothyroidism;
  14. Uncorrected electrolyte disturbances at the time of cardioversion (potassium level less than 3.5 mmol/l);
  15. Pregnancy and breastfeeding period.

Sites / Locations

  • Federal State Budgetary Institution NATIONAL MEDICAL RESEARCH CENTRE OF CARDIOLOGY NAMED AFTER ACADEMICIAN E.I.CHAZOV. of the Ministry of Health of the Russian FederationRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Refralone group

Arm Description

Patients with recurrent AF/AFL after catheter interventions to restore SR will be cardioverted with refralon

Outcomes

Primary Outcome Measures

Restoration of sinus rhythm
Restoration of SR within 24 hours from the moment of administration of the first dose of refraloRestoration of SR within 24 hours from the moment of administration of the first dose of refralon
Preservation of SR
Preservation of SR 24 hours after the first dose of refralon.
Ventricular arrhythmogenic effect
Registration of sustained and nonsustained (3 or more QRS) ventricular tachycardia or ventricular fibrillation after administration of drug
Increased QT interval (more than 500 ms)
The number of patients who have an increase in the QT interval (more than 500 ms) and the time during which the duration of the QT interval exceeded 500 ms.

Secondary Outcome Measures

Restoration of sinus rhythm within 6 hours
Restoration of SR within 6 hours from the moment of administration of the first dose of refralon
Number of patients recovering SR after minimal doses
Number of patients who recovered SR after minimal doses of refralon (5-10 μg/kg)
Reccurence after SR recovery
Absence of sustained (lasting more than 30 seconds) recurrences of AF/AFL within 24 hours after successful recovery of SR with refralon
Bradyarrhythmias (pauses and bradycardia)
Decrease in heart rate to less than 50bpm after administration of drug (refralon/amiodarone) during AF or after restoration of SR - the minimum heart rate, the duration of the maximum recorded pause and the time during which the heart rate was less than 50bpm will be recorded
Pauses more than 5 seconds
The presence of pauses for more than 5 seconds at the time of SR recovery or against the background of persistent AF/AT.

Full Information

First Posted
July 11, 2022
Last Updated
July 13, 2022
Sponsor
National Medical Research Center for Cardiology, Ministry of Health of Russian Federation
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1. Study Identification

Unique Protocol Identification Number
NCT05456204
Brief Title
Refralon in Patients With Recurrence Paroxysmal and Persistent Forms of Atrial Fibrillation Who Underwent Catheter Ablation
Official Title
Efficacy and Safety of Refralon in Patients With Recurrent Atrial Fibrillation and Atrial Flutter After Catheter Ablation.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 15, 2022 (Actual)
Primary Completion Date
September 10, 2024 (Anticipated)
Study Completion Date
October 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Medical Research Center for Cardiology, Ministry of Health of Russian Federation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
It is planned to evaluate the efficacy and safety of the class III antiarrhythmic drug refralon as a drug for pharmacological cardioversion in patients with recurrent atrial fibrillation (AF) and atrial flutter (AFL) after catheter ablation.
Detailed Description
Atrial fibrillation and atrial flutter are the most common arrhythmias among the adult population of the world, their share in the population is from 2 to 4% and continues to grow. Modern highly effective methods of minimally invasive surgical treatment of these types of arrhythmia are currently catheter radiofrequency ablation and balloon cryoablation of the pulmonary veins. According to the CABANA study, catheter interventions reduce the risk of recurrent AF/AFL by 47%, significantly improving arrhythmia tolerance and improving the quality of life of patients. An important problem is the recurrence of arrhythmia after the intervention, the frequency of recurrence of AF/AFL in the first 3 months after ablation (the so-called early recurrence) is 50-60%. In many patients, these recurrence are accompanied by severe clinical manifestations, which require pharmacological or electrical cardioversion. In order to restore sinus rhythm, electrical cardioversion is most often used, the effectiveness of which is 90-92%. An alternative to electrical cardioversion is pharmacological cardioversion, however, antiarrhythmic drugs used in wide clinical practice can restore sinus rhytm (SR) only in patients with recent AF paroxysms. In 2014, a new Russian class III antiarrhythmic drug, Refralon, was registered. The effectiveness of the Refralon as a means of cardioversion in patients with persistent AF/AFL is 90%, in patients with paroxysmal AF/AFL - 95%. At present, there is no information on the efficacy and safety of the use of refralon in patients with AF / AFL who underwent catheter ablation. The growing number of catheter ablation in the world dictates the to study new approaches to performing cardioversion in this cohort of patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrium; Fibrillation, Atrium; Flutter
Keywords
atrial fibrillation and flutter, paroxysmal and persistent atrial fibrillation and flutter, cardioversion AF, catheter radiofrequency ablation, Refralon, Niferidil, new antiarrhythmic drug, balloon cryoablation, reccurrence atrial fibrillation and flutter

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Refralone group
Arm Type
Other
Arm Description
Patients with recurrent AF/AFL after catheter interventions to restore SR will be cardioverted with refralon
Intervention Type
Drug
Intervention Name(s)
Pharmacological cardioversion with Refralon
Other Intervention Name(s)
Refralone
Intervention Description
the introduction of a 0.1% solution of refralon at a dose of 5 μg per 1 kg of body weight, diluted in 20 ml of saline intravenously for 2-3 minutes; in the absence of effect (SR recovery did not occur), after 15 minutes,repeated intravenous administration of a 0.1% solution of refralon at a dose of 5 μg per 1 kg of body weight (total dose of the drug 10 μg / kg of body weight); in the absence of effect (SR recovery did not occur),after 15 minutes, the next intravenous injection of a 0.1% solution of refralon at a dose of 10 μg per 1 kg of body weight (total dose of the drug 20 μg / kg of body weight); in the absence of effect (recovery of SR did not occur), after 15 minutes, repeated intravenous administration of a 0.1% solution of refralon at a dose of 10 μg per 1 kg of body weight. Thus, the maximum total dose of the drug will be 30 μg/kg of body weight.
Primary Outcome Measure Information:
Title
Restoration of sinus rhythm
Description
Restoration of SR within 24 hours from the moment of administration of the first dose of refraloRestoration of SR within 24 hours from the moment of administration of the first dose of refralon
Time Frame
24 hour
Title
Preservation of SR
Description
Preservation of SR 24 hours after the first dose of refralon.
Time Frame
24 hours
Title
Ventricular arrhythmogenic effect
Description
Registration of sustained and nonsustained (3 or more QRS) ventricular tachycardia or ventricular fibrillation after administration of drug
Time Frame
24 hours
Title
Increased QT interval (more than 500 ms)
Description
The number of patients who have an increase in the QT interval (more than 500 ms) and the time during which the duration of the QT interval exceeded 500 ms.
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
Restoration of sinus rhythm within 6 hours
Description
Restoration of SR within 6 hours from the moment of administration of the first dose of refralon
Time Frame
6 hours
Title
Number of patients recovering SR after minimal doses
Description
Number of patients who recovered SR after minimal doses of refralon (5-10 μg/kg)
Time Frame
24 hours
Title
Reccurence after SR recovery
Description
Absence of sustained (lasting more than 30 seconds) recurrences of AF/AFL within 24 hours after successful recovery of SR with refralon
Time Frame
24 hours
Title
Bradyarrhythmias (pauses and bradycardia)
Description
Decrease in heart rate to less than 50bpm after administration of drug (refralon/amiodarone) during AF or after restoration of SR - the minimum heart rate, the duration of the maximum recorded pause and the time during which the heart rate was less than 50bpm will be recorded
Time Frame
24 hours
Title
Pauses more than 5 seconds
Description
The presence of pauses for more than 5 seconds at the time of SR recovery or against the background of persistent AF/AT.
Time Frame
24 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 2. Patients with paroxysmal or persistent forms of AF/AFL and early (less than 90 days) or late (more than 90 days) arrhythmia recurrence after catheter radiofrequency ablation or balloon cryoablation of pulmonary veins. 3. Indications for SR recovery. 4. Consent of the patient. Exclusion Criteria: Arrhythmogenic effect of antiarrhythmic drugs III class in history; Chronic kidney disease with a decrease in glomerular filtration rate less than 30 ml / min / 1.73 m2; Chronic heart failure (functional class IV); Acute coronary syndrome; Bronchial asthma of an uncontrolled course and / or severe respiratory failure. The need for the use of drugs that increase the duration of the QT interval drugs without the possibility of withdrawal Atrioventricular blockade of 2-3 degrees (with the exception of patients with an implanted pacemaker); Dysfunction of the sinoatrial node (with the exception of patients with an implanted pacemaker); Bradysystolic atrial fibrillation (heart rate <50 beats/min); Duration of the QT interval >440 ms; Hemodynamic instability requiring emergency cardioversion; Contraindications to anticoagulant therapy; Thyrotoxicosis or decompensated hypothyroidism; Uncorrected electrolyte disturbances at the time of cardioversion (potassium level less than 3.5 mmol/l); Pregnancy and breastfeeding period.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nikolay Yu Mironov, PhD
Phone
84954146619
Email
nikmir.7ko@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Sergey P Golitsyn, MD
Email
golitsyn@umail.ru
Facility Information:
Facility Name
Federal State Budgetary Institution NATIONAL MEDICAL RESEARCH CENTRE OF CARDIOLOGY NAMED AFTER ACADEMICIAN E.I.CHAZOV. of the Ministry of Health of the Russian Federation
City
Moscow
ZIP/Postal Code
121552
Country
Russian Federation
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maksim A Zelberg
Phone
89166743504
Email
zelbergma@yandex.ru

12. IPD Sharing Statement

Learn more about this trial

Refralon in Patients With Recurrence Paroxysmal and Persistent Forms of Atrial Fibrillation Who Underwent Catheter Ablation

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