Clinical Benefits of the Closed Loop Stimulation in Sinus Node Disease (B3)

Biotronik

Status: Terminated

Conditions: Sinus Node Disease

Treatments: Device: DDD+CLS; Device: DDD(R)

Study type: Interventional

Funder types: Industry

Identifiers

NCT02579889

BA104

Details and patient eligibility

About

The study is designed as a multi-center, international, prospective, parallel, randomized, single blinded trial comparing the time to first primary endpoint event (Sustained Paroxysmal AF/Persistent AF or stroke/TIA) occurrence in a follow up period of 3 years, between Closed Loop Stimulation (CLS) ON versus OFF, on top of a DDD pacing in patients with pacemaker or ICD indication who require dual-chamber pacing due to sinus node disease (SND), with or without atrioventricular (AV) block.

Full description

The benefits of rate-responsiveness on top of dual-chamber pacing still need to be definitively assessed in Sinus Node Dysfunction (SND). Although many rate responsive (RR) sensors have been developed, no large clinical trials evaluated their benefits in terms of clinical endpoints such as clinically relevant atrial fibrillation (AF) and stroke. Electromechanical sensors (piezoelectric accelerometers) have been widely used for their simplicity and overall reliability. However there is some evidence indicating the Closed Loop Stimulation as one of the more efficient and physiological sensors.

Two randomized clinical studies have been conducted so far, showing that in the Brady-Tachy Syndrome the CLS algorithm was associated with a significantly lower overall atrial arrhythmia burden as compared both with a DDDR mode based on a standard accelerometric sensor and an atrial overdrive approach.

Both studies yielded consistent results, albeit with a parallel and intraindividual comparison designs, respectively. The atrial arrhythmic burden is an important but surrogate endpoint, not necessarily related to long-term clinical outcome. The CLS effects on AF (if any) should be investigated in terms of time to first new onset of clinically relevant AF.

In the light of these considerations, it appears interesting to run a large randomized study coherently collecting data on the overall clinical benefit of CLS, primarily in terms of AF and stroke, in a population indicated for pacemaker or ICD and needing dual-chamber pacing due to SND.

Enrollment: 1,390 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients with Class I or II recommendations for permanent pacing due to SND, with or without AV block according to the current guidelines;
• Patients for whom dual-chamber pacing is indicated or preferred;
• Patients with an optimized and stable antiarrhythmic medical therapy at the time of enrolment;
• Closed Loop Stimulation function was not previously activated;
• No stroke events from implant;
• Patient implanted for the first time;

Exclusion criteria

• Permanent AF (PermAF)
• NYHA Class IV Heart Failure
• Stage V kidney dysfunction
• Any indication to Cardiac Resynchronization Therapy (CRT)
• Life expectancy < 1
• Minors
• Pregnant or breast-feeding patients
• Participation in another interventional trial
• Atrial fibrillation ablation (left pulmonary veins) or other cardiac surgery < 3 m

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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1,390 participants in 2 patient groups

Active group - CLS ON

Experimental group

Description:

Device will be programmed in a dual-chamber DDD pacing mode with the Closed Loop Stimulation (CLS) function ON; Intervention: DDD+CLS

Treatment:

Device: DDD+CLS

Control group - CLS OFF

Active Comparator group

Description:

Device will be programmed in a dual-chamber DDD(R) pacing mode with the Closed Loop Stimulation (CLS) function OFF

Treatment:

Device: DDD(R)