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Cardiac Contractility Modulation in Patients With Chronic Heart Failure and the Various Forms of Atrial Fibrillation

Primary Purpose

Heart Failure, Atrial Fibrillation, Left Ventricular Ejection Fraction

Status
Completed
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
optimizer smart
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 Heart Failure focused on measuring Cardiac contractility modulation, Atrial Fibrillation, Heart Failure, Narrow QRS Complex, left ventricular ejection fraction

Eligibility Criteria

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

Inclusion Criteria:

  • Documented HFrEF (20-40%)
  • NYHA FC II-III for at least 3 months before screening
  • AF
  • Optimal CHF therapy and the absence of decompensations in ≥ 1 month.

Exclusion Criteria:

  • Refusal to participate in the study
  • Placement on the heart transplant waiting list, or post heart transplantation
  • Terminal CHF
  • Co-morbid diseases that may adversely affect the safety and / or efficacy of treatment
  • Recent surgical intervention or trauma
  • Medical conditions that limit life expectancy to 1 year.

Sites / Locations

  • Alfiya Safiullina

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Optimizer device

Without Optimizer device

Arm Description

100 patients were enrolled sequentially, 100 patients were implanted with an optimizer smart against the background of optimal drug therapy for heart failure 100 patients were implanted with a CCM Optimizer device without an atrial lead, per the protocol specifications recived optimal drug therapy CHF The following studies were performed in the 100 patients with CHF and AF before implantation of the MCC device and after 2 and 6 и 12 months of follow-up: 12-channel ECG with an estimate of the width of the QRS complex, transthoracic EchoCG,Speckle-tracking EchoCG,Myocardial work, 6-minute walk test, determination of the level of Pro-natriuretic N-terminal peptide (NT-proBNP), Holter ECG, and a questionnaire based on the Minnesota quality of life questionnaire for patients with CHF (MHFLQ).

100 patients were enrolled sequentially,100 patients received only optimal drug therapy for chronic heart failure 100 patients ( Without Optimizer device ) with CHF and AF before study and after 2 and 6 и 12 months of follow-up: 12-channel ECG with an estimate of the width of the QRS complex, transthoracic EchoCG,Speckle-tracking EchoCG,Myocardial work, 6-minute walk test, determination of the level of Pro-natriuretic N-terminal peptide (NT-proBNP), Holter ECG, and a questionnaire based on the Minnesota quality of life questionnaire for patients with CHF (MHFLQ).

Outcomes

Primary Outcome Measures

cardiovascular death + hospitalization due to decompensation of HF
Number of Participants with cardiovascular death + hospitalization due to decompensation of HF

Secondary Outcome Measures

death from all causes
Number of Participants with death from all causes
hospitalization for any reason
Number of Participants with hospitalization for any reason
development of AF paroxysm in patients with paroxysmal AF
Number of Participants with development of AF paroxysm in patients with paroxysmal AF
worsening of the course of CHF, which required an outpatient visit and increased doses of diuretics
Number of Participants with worsening of the course of CHF, which required an outpatient visit and increased doses of diuretics
complications that required removal of the MCC
Number of Participants with complications that required removal of the MCC

Full Information

First Posted
January 26, 2022
Last Updated
September 20, 2022
Sponsor
National Medical Research Center for Cardiology, Ministry of Health of Russian Federation
Collaborators
Ministry of Health, Russian Federation
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1. Study Identification

Unique Protocol Identification Number
NCT05550792
Brief Title
Cardiac Contractility Modulation in Patients With Chronic Heart Failure and the Various Forms of Atrial Fibrillation
Official Title
Cardiac Contractility Modulation in Patients With Chronic Heart Failure and the Various Forms of Atrial Fibrillation
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
August 31, 2018 (Actual)
Primary Completion Date
December 10, 2019 (Actual)
Study Completion Date
March 30, 2022 (Actual)

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
Collaborators
Ministry of Health, 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
Yes

5. Study Description

Brief Summary
Chronic heart failure (CHF) is a global pandemic which affects around 26 million people worldwide and develops in 10% of people over 70 years . According to the results of the EPOCHA-CHF study, CHF is detected in 7-10% of cases in the Russian Federation . Atrial fibrillation (AF) is the most common arrhythmia in patients with both preserved (HFpEF) and reduced ejection fraction (HFrEF) heart failure. The prognostic impact of AF on CHF is negative, including the significant increase in mortality and hospitalization. One of the common causes of decompensation of CHF is AF. The debut of AF in CHF is one of the markers of disease progression. Rapid development in interventional cardiology due to the invention of cardiac catheter technologies during the last decades provided a new option for non-pharmacological treatment of CHF. Nowadays the use of electrophysiological methods of treatment can significantly improve the prognosis of CHF. Pacemakers, cardiac resynchronization devices, and cardioverter defibrillators are the most commonly implanted devices in patients with CHF. In 2014, the European Society of Cardiology presented a report of the European Heart Rhythm Association on the use of new devices for CHF, including the Optimizer device for delivery of cardiac contractility modulation therapy (CCM) . It is worth noting that CCM is a new step in the CHF treatment. This device is of proven benefit to patients with symptomatic heart failure on optimal medical therapy who do not qualify for cardiac resynchronization therapy. Multiple studies of CCM show clinical improvement with this therapy, including metrics such as peak VO2, 6MW, and NYHA functional class. However, the vast majority of patients enrolled in these studies were patients in sinus rhythm. As the technology progressed and the need for the trial sensing led wanted, further experiences incorporated patients with AF. A new generation of devices (Optimizer Smart®), which does not require the implantation of an atrial electrode made it possible to implant CCM in patients with AF. The present trial demonstrates the results of a pilot study conducted in National Medical Research Center of Cardiology Ministry of Health of the Russian Federation which compares the efficacy of CCM in patients with AF and ischemic and non-ischemic CHF compared to patients who received only optimal drug therapy CHF
Detailed Description
Background: Chronic heart failure (CHF) and atrial fibrillation (AF) often coexist and lead to severe decompensation of patients' lifestyle. Nowadays device therapy such as cardiac contractility modulation (CCM), which is used in addition to medical treatment, can significantly impact further prognosis and outcomes of patients with such comorbidities. Methods: In the National Medical Research Center of Cardiology we conducted a study dedicated to investigating the efficacy of CCM in patients with CHF and AF. 200 patients with Hf and AF were included in the study and were divided into two groups according to implantation of a heart contractility modulation device and optimal drug therapy. 100 patients were implanted with a CCM Optimizer device without an atrial lead, per the protocol specifications ( 1 group) and 100 patients ( 2 group) received only optimal drug therapy CHF The following studies were performed in the 200 patients with CHF and AF before implantation of the MCC device and after 2 and 6 и 12 months of follow-up: 12-channel ECG with an estimate of the width of the QRS complex, transthoracic EchoCG, Speckle-tracking EchoCG, Myocardial work, 6-minute walk test, determination of the level of Pro-natriuretic N-terminal peptide (NT-proBNP), Holter ECG, and a questionnaire based on the Minnesota quality of life questionnaire for patients with CHF (MHFLQ),Perfusion Single-Photon Emission Computed Tomography All patients received long-term optimal drug therapy for CHF before surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Atrial Fibrillation, Left Ventricular Ejection Fraction
Keywords
Cardiac contractility modulation, Atrial Fibrillation, Heart Failure, Narrow QRS Complex, left ventricular ejection fraction

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Optimizer device
Arm Type
Active Comparator
Arm Description
100 patients were enrolled sequentially, 100 patients were implanted with an optimizer smart against the background of optimal drug therapy for heart failure 100 patients were implanted with a CCM Optimizer device without an atrial lead, per the protocol specifications recived optimal drug therapy CHF The following studies were performed in the 100 patients with CHF and AF before implantation of the MCC device and after 2 and 6 и 12 months of follow-up: 12-channel ECG with an estimate of the width of the QRS complex, transthoracic EchoCG,Speckle-tracking EchoCG,Myocardial work, 6-minute walk test, determination of the level of Pro-natriuretic N-terminal peptide (NT-proBNP), Holter ECG, and a questionnaire based on the Minnesota quality of life questionnaire for patients with CHF (MHFLQ).
Arm Title
Without Optimizer device
Arm Type
No Intervention
Arm Description
100 patients were enrolled sequentially,100 patients received only optimal drug therapy for chronic heart failure 100 patients ( Without Optimizer device ) with CHF and AF before study and after 2 and 6 и 12 months of follow-up: 12-channel ECG with an estimate of the width of the QRS complex, transthoracic EchoCG,Speckle-tracking EchoCG,Myocardial work, 6-minute walk test, determination of the level of Pro-natriuretic N-terminal peptide (NT-proBNP), Holter ECG, and a questionnaire based on the Minnesota quality of life questionnaire for patients with CHF (MHFLQ).
Intervention Type
Device
Intervention Name(s)
optimizer smart
Intervention Description
The CCM implantation procedure was performed in the right precordial region of the chest (the right subclavian area). Two active fixation Ingevity leads (Boston Scientific) were advanced via the right subclavian vein into the right ventricle (RV) and actively fixed to the right ventricular septum for ventricular sensing and delivery of CCM signals.
Primary Outcome Measure Information:
Title
cardiovascular death + hospitalization due to decompensation of HF
Description
Number of Participants with cardiovascular death + hospitalization due to decompensation of HF
Time Frame
12 month
Secondary Outcome Measure Information:
Title
death from all causes
Description
Number of Participants with death from all causes
Time Frame
12 month
Title
hospitalization for any reason
Description
Number of Participants with hospitalization for any reason
Time Frame
12 month
Title
development of AF paroxysm in patients with paroxysmal AF
Description
Number of Participants with development of AF paroxysm in patients with paroxysmal AF
Time Frame
12 month
Title
worsening of the course of CHF, which required an outpatient visit and increased doses of diuretics
Description
Number of Participants with worsening of the course of CHF, which required an outpatient visit and increased doses of diuretics
Time Frame
12 month
Title
complications that required removal of the MCC
Description
Number of Participants with complications that required removal of the MCC
Time Frame
12 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Documented HFrEF (20-40%) NYHA FC II-III for at least 3 months before screening AF Optimal CHF therapy and the absence of decompensations in ≥ 1 month. Exclusion Criteria: Refusal to participate in the study Placement on the heart transplant waiting list, or post heart transplantation Terminal CHF Co-morbid diseases that may adversely affect the safety and / or efficacy of treatment Recent surgical intervention or trauma Medical conditions that limit life expectancy to 1 year.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alfiya Safiullina, phd
Organizational Affiliation
National Medical Research Center for Cardiology, Ministry of Health of Russian Federation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Alfiya Safiullina
City
Moscow
ZIP/Postal Code
121552
Country
Russian Federation

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33346425
Citation
Uskach TM, Safiullina AA, Sapel'nikov OV, Amanatova VA, Nikolaeva OA, Grishin IR, Nazarov BM, Tereshchenko SN. [Modulation of cardiac contractility in patients with chronic heart failure and atrial fibrillation]. Ter Arkh. 2020 Oct 14;92(9):8-14. doi: 10.26442/00403660.2020.09.000598. Russian.
Results Reference
result
PubMed Identifier
35057719
Citation
Dobrovolskaya SV, Saidova MA, Safiullina AA, Uskach TM, Tereshchenko SN. [Evaluation of the effectiveness of the chronic heart failure therapy using the device cardiac contractility modulation according to the new non-invasive method of the myocardium work analysis]. Kardiologiia. 2021 Dec 31;61(12):31-40. doi: 10.18087/cardio.2021.12.n1849. Russian.
Results Reference
result

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Cardiac Contractility Modulation in Patients With Chronic Heart Failure and the Various Forms of Atrial Fibrillation

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