Efficacy and Safety Evaluation of Refralon®, Concentrate for Solution for Intravenous Injection in Patients With Paroxysmal and Persistent Atrial Fibrillation and Flutter

Sponsor
R-Pharm (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05773170
Collaborator
FSBI "National Medical Research Center of Cardiology named after academician E.I.Chazov" of the Ministry of Health of the Russian Federation (Other)
1,500
32
6.6
46.9
7.1

Study Details

Study Description

Brief Summary

The goal of this retrospective registry is to evaluate the efficacy and safety of Refralon®, concentrate for solution for intravenous injection, as chemical cardioversion in patients with paroxysmal and persistent atrial fibrillation and flutter in routine clinical practice.

The main questions it aims to answer are:
  • What is the incidence of sinus rhythm restoration within 6 hours in patients with paroxysmal atrial fibrillation (AF)/atrial flutter (AFL) after the first dose of Refralon®?

  • What is the incidence of sinus rhythm restoration within 24 hours in patients with persistent AF/AFL after the first dose of Refralon®?

Detailed Description

The registry is a retrospective multicenter observational study in patients with paroxysmal and persistent forms of AF and AFL who underwent chemical cardioversion with Refralon® in a hospital setting.

After the compliance with the inclusion criteria and the absence of exclusion criteria based on medical documentation, the patient data will be collected from medical documentation available for the analysis into a unified electronic case report form (eCRF).

Alongside the study therapy, all the patients must receive an adequate anticoagulant therapy in accordance with the current clinical guidelines of the Ministry of Health of the Russian Federation. After chemical cardioversion, patients were followed up and examined as a part of routine clinical practice. The examination data will be used for this study analysis. No additional therapeutic or diagnostic procedures are provided by the analysis protocol.

Study patient follow-up period was 24 hours from the Refralon® first dose administration.

The patients' data collection is planned for 8 months. It is planned to enroll 1500 patients with persistent and paroxysmal AF and AFL, meeting the inclusion/exclusion criteria. If necessary, it is possible to extend the registry data collection period to include the planned number of patients.

Approximately in 3 and 6 months from the registry initiation (but not earlier than after the inclusion of 150 patients into the registry), an interim collected data analysis can be performed in order to preliminary assess the Refralon® efficacy and safety data in this study, as well as to identify the potential data entry errors.

Study Design

Study Type:
Observational
Anticipated Enrollment :
1500 participants
Observational Model:
Case-Only
Time Perspective:
Retrospective
Official Title:
Retrospective Registry for the Efficacy and Safety Evaluation of Refralon®, Concentrate for Solution for Intravenous Injection in Patients With Paroxysmal and Persistent Atrial Fibrillation and Flutter
Actual Study Start Date :
Nov 11, 2022
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Jun 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Pharmacological cardioversion with Refralon

Refralon® 0.1% solution administration at a dose of 10 μg/kg of body weight intravenously (IV) for 2-3 minutes; It is allowed to divide the first Refralon® bolus into two consecutive injections: the first dose administration - 5 μg/kg of body weight, if the AF/AFL persists, administer the second dose - 5 μg/kg of body weight (total dose 10 μg/kg) in 15 minutes. If no effect is registered (no sinus rhythm restoration), repeat IV administration of Refralon® 0.1% solution at a dose of 10 μg/kg of body weight (total dose: 20 μg/kg of body weight) in 15 minutes; If no effect is registered, repeat IV administration of Refralon® 0.1% solution at a dose of 10 μg/kg of body weight (total dose: 30 μg/kg of body weight) in 15 minutes. In case of AF/AFL recurrence after the sinus rhythm restoration (with no contraindications), it is possible to re-administer Refralon®, while the maximum total drug daily dose (from the first administration) should not exceed 30 μg/kg of body weight.

Drug: Refralon
1 mg/ml concentrate for solution for intravenous injection. (Prior to the administration, 2 mL of Refralon® must be diluted to 20 mL in 0.9 % sodium chloride).
Other Names:
  • 4-nitro-N-[(1RS)-1-(4-fluorophenyl)-2-(1-ethylpiperidin-4-yl)ethyl]benzamide hydrochloride
  • Niferidyl
  • Outcome Measures

    Primary Outcome Measures

    1. Incidence of sinus rhythm restoration [up to 6 hours]

      Incidence of sinus rhythm restoration within 6 hours in patients with paroxysmal AF/AFL after the first dose of Refralon®

    2. Incidence of sinus rhythm restoration [up to 24 hours]

      Incidence of sinus rhythm restoration within 24 hours in patients with persistent AF/AFL after the first dose of Refralon®

    Secondary Outcome Measures

    1. Time from the Refralon® administration start to the sinus rhythm restoration [from Refralon® administration to the sinus rhythm restoration, up to 24 hours]

    2. Incidence of sinus rhythm maintenance [up to 24 hours]

      Incidence of sinus rhythm maintenance in patients 24 hours after the first Refralon® dose

    3. Incidence of AF/AFL sustained recurrences [up to 24 hours]

      Incidence of AF/AFL sustained (for more than 30 seconds) recurrences within 24 hours after the successful cardioversion with Refralon®

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Diagnosis: paroxysmal or persistent atrial fibrillation or flutter;

    • A chemical cardioversion procedure performed with Refralon® in a hospital setting.

    Exclusion Criteria:
    • Congenital or acquired QT interval prolongation in the electrocardiogram (ECG) in 12 standard leads for more than 440 ms at the time of cardioversion;

    • Bradysystolic atrial fibrillation or flutter (mean heart rate < 50 bpm or pauses > 3 sec, registered on the ECG or identified by the results of 24-hour Holter ECG monitoring, except for the cases of its correction by a cardiac pacemaker at the time of cardioversion;

    • Sick sinus syndrome (sinus bradycardia, sinoatrial blockade), previously registered as associated with sinus rhythm, except for the cases of its correction with a cardiac pacemaker at the time of cardioversion;

    • Degree II - III atrioventricular blockade, two- and three-beam blockade with no cardiac pacemaker at thentime of cardioversion;

    • Acute myocardial infarction period at the time of cardioversion;

    • Acute period after coronary artery bypass grafting (CABG) or other cardiac surgery (at least 7 days after CABG at the time of cardioversion);

    • Decompensated or severe chronic heart failure (III-IV functional class according to New York Heart Association (NYHA) classification) at the time of cardioversion;

    • Uncontrolled bronchial asthma, severe respiratory failure at the time of cardioversion;

    • Pregnancy and breastfeeding at the time of cardioversion;

    • Administration of Class IA antiarrhythmic drugs (quinidine, hydroquinidine, disopyramide, procainamide) at the time of cardioversion;

    • Class III antiarrhythmic drugs administration at the time of cardioversion;

    • Cardiac glycosides administration at the time of cardioversion;

    • Administration of QT-prolonging drugs at the time of cardioversion;

    • Heart rate < 50 bpm, pauses > 3 seconds on the ECG or Holter ECG monitoring (HM-ECG) during wakefulness at the time of cardioversion;

    • Hyperthyroidism or decompensated hypothyroidism (thyroid stimulating hormone (TSH) < lower limit of normal or > 2 upper limits of normal) at the time of cardioversion;

    • Uncorrectable electrolyte disorders (potassium level less than 3.5 mmol/L) at the time of cardioversion;

    • Identified contraindications to the sinus rhythm restoration at the time of cardioversion;

    • Blood clots in the heart cavities or spontaneous grade III-IV echo contrast at the time of cardioversion according to transesophageal echocardiography;

    • The need for electrical cardioversion due to the patient's hemodynamic instability at the time of cardioversion.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Federal State Budgetary Educational Institution of Higher Education "Bashkir State Medical University" of the Ministry for Healthcare of the Russian Federation Ufa Bashkortostan Republic Russian Federation 450059
    2 State Budgetary Healthcare Institution of Republic of Bashkortostan "City Hospital Clinical Hospital № 21" Ufa Bashkortostan Republic Russian Federation 450071
    3 State Autonomous Healthcare Institution of the Kemerovo Region "Novokuznetsk City Clinical Hospital № 1" Novokuznetsk Kemerovo Region Russian Federation 654057
    4 State Budgetary Healthcare Institution of Sverdlovsk Region "Scientific-practical center of specialized typed of medical care "URAL INSTITUTE OF CARDIOLOGY" Yekaterinburg Sverdlovsk Region Russian Federation 620063
    5 "First Clinical Medical Center" LLC Kovrov Vladimir Region Russian Federation 601911
    6 The Regional State Budgetary Healthcare Institution "St. Joseph Belgorod Regional Clinical Hospital" Belgorod Russian Federation 308007
    7 State budgetary Healthcare Institution "Cardiological Dispensary" Ivanovo Russian Federation 153012
    8 Federal State Budgetary Institution "National Medical Research Center for Therapy and Preventive Medicine" of the Ministry of Healthсare of the Russian Federation Moscow Russian Federation 101990
    9 State Budgetary Healthcare Institution "City Clinical Hospital named after I.V. Davydovsky of Moscow Healthcare Department" Moscow Russian Federation 109240
    10 Federal State Budgetary Institution "Clinical hospital № 1" administrative Department of the President of the Russian Federation Moscow Russian Federation 121352
    11 Federal State Budget Institution "A.N. Bakulev National Medical Research Center of Cardiovascular Surgery" of the Ministry of Health of the Russian Federation Moscow Russian Federation 121552
    12 State Budgetary Healthcare Institution of the Novosibirsk Region "Novosibirsk Regional Clinical Cardiology Dispensary" Novosibirsk Russian Federation 630047
    13 State Budgetary Healthcare Institution of the Novosibirsk region "City Clinical Hospital № 2" Novosibirsk Russian Federation 630051
    14 State Budgetary Healthcare Institution of the Perm Region "Clinical Cardiological Dispensary Perm Russian Federation 614002
    15 State Budgetary Institution of the Ryazan region "Regional Clinical Cardiology Dispensary" Ryazan Russian Federation 390026
    16 The State Budgetary Healthcare Institution of the Samara Region "Samara Regional Clinical Cardiology Dispensary named after V.P. Polyakov" Samara Russian Federation 443070
    17 Samara City Clinical Hospital № 1 named after N.I. Pirogov Samara Russian Federation 443096
    18 State Health Care Institution "Regional Cardiology Clinic" Saratov Russian Federation 410039
    19 St. Petersburg State Budgetary Healthcare Institution "Hospital for War Veterans" St. Petersburg Russian Federation 193079
    20 Federal State Budgetary Institution "National Medical Research Center (NMIC) named after V. A. Almazov" Ministry of Health Russia St. Petersburg Russian Federation 197341
    21 The Saint Petersburg State Health Care Establishment the City Hospital № 40 of the Resort District St. Petersburg Russian Federation 197706
    22 Tambov Regional State Budgetary Healthcare Institution "S.S. Bryukhonenko City Hospital of Michurinsk" Tambov Russian Federation 393760
    23 Cardiology Research Institute, Federal State Budgetary Scientific Institution "Tomsk National Research Medical Center of the Russian Academy of Sciences" Tomsk Russian Federation 634012
    24 State health institution City Hospital № 13 Tula (Tula regional cardiological dispensary) Tula Russian Federation 300065
    25 The State Budgetary Healthcare Institution of the Tver region "Regional Clinical Hospital" Tver Russian Federation 170036
    26 The State Budgetary Healthcare Institution of the Vladimir Region "State Hospital № 4" Vladimir Russian Federation 600020
    27 The State Budgetary Healthcare Institution "Volgograd Regional Clinical Cardiology Center" Volgograd Russian Federation 400008
    28 Budget Healthcare Institution of the Vologda Region "Vologda Regional Clinical Hospital" Vologda Russian Federation 160002
    29 The State Healthcare Institution "Voronezh Regional Hospital № 1" Voronezh Russian Federation 394066
    30 The State Budgetary Health Care Institution of the Yaroslavl Region "Regional Clinical Hospital" Yaroslavl Russian Federation 150062
    31 State Budgetary Healthcare Institution "Sakhalin Regional Clinical Hospital" Yuzhno-Sakhalinsk Russian Federation 690034
    32 State Budgetary Healthcare Institution of the Sakhalin region "Yuzhno-Sakhalinsk City Hospital named after F.S. Ankudinov" Yuzhno-Sakhalinsk Russian Federation 693010

    Sponsors and Collaborators

    • R-Pharm
    • FSBI "National Medical Research Center of Cardiology named after academician E.I.Chazov" of the Ministry of Health of the Russian Federation

    Investigators

    • Study Director: Mikhail Samsonov, Chief Medical Officer, R-Pharm

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    R-Pharm
    ClinicalTrials.gov Identifier:
    NCT05773170
    Other Study ID Numbers:
    • CC01897112
    First Posted:
    Mar 17, 2023
    Last Update Posted:
    Mar 17, 2023
    Last Verified:
    Mar 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by R-Pharm
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 17, 2023