Postmarketing, Prospective, Multicenter, Randomized and Blinded Study to Evaluate the Superior Efficacy of Cardiac Resynchronization Using the SyncAVTM Algorithm
Postmarketing, Prospective, Multicenter, Randomized and Blinded Study to Evaluate the Superior Efficacy of Cardiac Resynchronization Using the SyncAVTM Algorithm
Heart Failure (HF) is a cardiovascular disease secondary to a structural and / or functional alteration of the heart that prevents its correct function.
The Cardiac resynchronization therapy (CRT) aims to restore atrioventricular, inter and intraventricular synchrony in patients with systolic HF and wide depolarization of the ventricles (QRS). Although CRT has been shown to be effective, the rate of non-responders is high (30-50%).
One of the proposed reasons for the lack of response to the CRT is the lack of intrinsic conduction, since most of the time CRT is administered using biventricular stimulation (BiV). One of the limitations to achieve ventricular fusion are the dynamic physiological variations of the auriculo-ventricular (AV) interval.
The SyncAVTM algorithm is a new dynamic algorithm that manages to adjust the AV intervals outside the clinic.
The design of the present clinical study is post-marketing, prospective, multicenter, randomized and blind for the patient and the central echocardiography laboratory.
The objective of this study is to assess whether CRT with ventricular stimulation with fusion using the SyncAVTM algorithm is superior to CRT with conventional BiV stimulation in the population for which its use is foreseen.
The data will be collected in at least the Selection / Baseline Visit and in the Visit of Follow-up at 6 Months.
The study population are subjects to whom an Abbott Medical CRT has been implanted with SyncAVTM® Stimulation function that go to the participating sites in the study.
The main objective of the study is to assess whether CRT with ventricular stimulation with fusion using the SyncAVTM algorithm is superior to CRT with BiV stimulation conventional in terms of the rate of responders.
The main endpoint is the determination of significant differences between conventional BiV stimulation and ventricular stimulation with fusion using the SyncAVTM algorithm in terms of the percentage of patients responding to CRT therapy with echocardiogram.
The duration of the clinical study is estimated at 24 months with a recruitment period of 18 months and a patient follow-up of 6 months. The number of subjects that is planned to be recruited is 176. The inclusion will be competitive and there is no inclusion number determined per site.
Study design The study is designed post-marketing, prospective, multicenter, randomized and blind for the patient and for the Core-laboratory of the echocardiogram (ECO) department. Has this design is post- marketing since it is a sanitary product with European Committee (CE) marking that is already commercialized and will be used in the study according to its instructions for use. Is a blind study since neither the participant subject nor the Core-laboratory of the ECO (person in charge to assess the main variable of the study) know the treatment that has been randomized the subject, it is a randomized study because the group assignment of each subject is done randomly 1:1.
Study evaluation Evaluation of the risk and benefits of the study: The following will be taking into account
Expected clinical benefits:
Expected adverse effects of the product: bleeding/acute hemorrhage, gas aeration, acceleration of arrythmias, cysts formation, erosion,exacerbation of cardiac insufficiency, venous or cardiac perforation, excessive fibrous tissue development, bruising, histotoxic reactions, infection, keloid formation, myocardial irritability, infection, hematoma, excessive bleeding, local tissue reaction, loss of stimulation and/or detection due to migration or mechanical malfunction, myocardial irritability, stimulation of the nerve, etc. All those events are inherent to the implant of the device for cardiac resynchronization therapy
Risk associated with participation in this clinical trial: It is expected that the risks associated with the use of the SyncAVTM stimulation algorithm be comparable to the risks associated with other types of ventricular pacing, and therefore, the risks associated with the use of the stimulation algorithm are expected SyncAVTM will not differ from the risks associated with the different modes of Conventional stimulation available. Patients will be included in the study after the successful implantation of a CRT device, whose indication will be made clinically based on the guidelines current clinical practice of the European Society of Cardiology (ESC).
Possible interactions with concomitant medical treatments and / or Simultaneous medical interventions:
No interaction with concomitant pharmacological treatments and / or medical interventions simultaneous, apart from those that occur in the usual treatment with any CRT device. All participants will be candidates for the implantation of a CRT device and will be included in the clinical study once the device has been implanted successfully.
Main Valuation criterion:
The main endpoint of the study is to determine if there are differences significant differences between conventional BiV stimulation and ventricular pacing with fusion using the SyncAVTM algorithm in terms of the percentage of patients responders to CRT therapy
The positive response to CRT is defined as an improvement> 15% in the Systolic Volume End in the Left Ventricle (VSFVI) 6 months after implantation, evaluated by echocardiography.
▪ Secondary rating criterion The secondary endpoints of this study are differences between:
SAFETY ASSESSMENT The safety of the stimulation algorithms will be evaluated by collecting and registering of any dysfunction, alteration of the features or performance of the product that could or could have led to the death or serious deterioration of the state of health of a patient or a user. Therefore, safety has as an evaluation criterion the Record and analyze the frequency and intensity of adverse incidents that occur throughout the study. For the evaluation of safety, the Population of Security (PS).
Evaluation of effectiveness The superior efficacy of CRT with ventricular stimulation with fusion through SyncAVTM algorithm versus CRT with conventional BiV stimulation will be studied comparing the results of the stimulation logarithms between the two branches of the study (stimulation by SyncAVTM algorithm and conventional BiV stimulation).The ultimate goal of the study is to determine the percentage of responding patients and not respondents The response of patients to CRT will be evaluated taking into account the reduction of VSFVI. Patients will be classified as responders. have documented a reduction in VSFVI of at least 15% compared to the data collected in the Basal situation without stimulation. The evaluation of the effectiveness will be analyzed with the Population of Intent to Treat (ITT) and Population by Protocol (PP).
Sample size The calculation of the sample size is based on the main variable: the proportion of responders to CRT at 6 months with the SyncAV function activated at the start of the study.
The main variable of the study is the response to re-synchronization, understood as a dichotomous variable that takes the values: Yes / No. In the study there will be two randomization groups, and the response rate of the control group is set at 65% of the patients, while that of the study group will be 77%, that is, 12% higher. As statistical criteria for the estimation of the sample size, it was used a confidence level of 95%, a margin of non-inferiority δ = 0 and a power a priori of 80%. The statistical technique used for the analysis of the main variable is a test χ 2
The formula used to calculate the sample size is as follows (Chow, Shao and Wang, 2008): In addition, it is assumed that 5% of patients may be lost due to loss of follow-up and 8% due to exitus. For the calculation of the sample size, the R-studio software (version 1.0.153). Applying the formula, the sample size is 77 patients per group, that is, a total of 154 patients. However, 22 more must be added (11 more patients in each group) due to possible loss of follow-up and due to death.
Considering all the above information, the expected sample size is of 176 patients, 88 patients would be randomized to the control group and 88 to the group of study.
Using an exact binomial test of a unilateral sample, with a level of significance of 95%, a total of 176 patients would be necessary to reach a 80% power.
To detect a difference of 12% between the two responder rates, it is It is necessary that a total of 176 patients have analysable data at 6 months.
Based on clinical experience, it is assumed that some patients will abandon the study (5% during the first 6 months of implantation, 8% due to exitus)
STATISTICAL ANALYSIS
Statistical design, hypothesis, method and analytical procedures:
The analysis of the main variable will be based on the intention to treat principle (ITT), including all deviations from the Protocol. There will also be a secondary analysis per Protocol (PP), excluding all deviations of the Protocol. If the results obtained in these analyzes were different, an exploration of the data will be done in search of the reasons. In the analysis of the main variable will be evaluated the following hypothesis of inequality:
All results will be expressed according to the corresponding intervals confidence of 97.5% and the values p. P values less than 2.5% are will consider significant.
Inclusion Criteria:
Patients older than 18 years.
Patients who state that they understand the study and are willing to participate in it by signing the corresponding Informed Consent form.
Patients who have been implanted with an Abbott Medical ® CRT with SyncAVTM stimulation function under the current ESC Class I or Class II-a indications for the implantation of CRT (including updates from pacemakers or single-chamber or double-chamber of an implantable cardioverter-defibrillator (ICDs)).
In sinus rhythm during the Basal visit.
Patients with Left Branch Block (LBB) defined as:
LVEF <35% being under optimal medical treatment
PR Baseline <250 ms without BAV of 2nd or 3rd grade.
Patients who are willing to meet all the requirements of the study and who have the ability to do it.
Exclusion Criteria: