About this trial
The PROTECT-HF multi-centre randomised controlled trial will compare two different pacing approaches for treating patients with slow heart rates. In it the investigators will compare a long-standing standard approach for pacing; right ventricular pacing, with a new form of pacing, physiological pacing (His and Left bundle area pacing) in 2600 patients.
Patients will be allocated at random to receive either right ventricular pacing or physiological pacing. Endpoint measurements will be undertaken at baseline, and at six-monthly intervals post-randomisation. Treatment allocation will be blinded to the endpoint assessor and the patient.
Recruitment and pacemaker implantation will be carried out at each participating centre. The primary analysis will be intention to treat. The investigators will also perform an on-treatment analysis.
2048 patients are needed to detect the expected effect size with 85% power. A total of 2600 patients will be recruited to allow for patient drop-out and crossover.
500-patient sub-study will assess within patient, and between groups, echocardiographic changes over a 24-month period to try and improve mechanistic understanding of PICM (Pacing Induced Cardiomyopathy).
Eligibility criteria
Qualifiers
Permanent or intermittent 3rd degree AV block
Permanent or intermittent Mobitz type II AV block
First Degree AV block with a pacing indication
Slow chronic Atrial Fibrillation or Proposed AV node ablation
Disqualifiers
Patients who are likely to only need occasional ventricular pacing, i.e. those with isolated sick sinus syndrome.
Pregnant women.
Unable to provide informed consent.
Those with comorbidity leading to a life expectancy <1year.
Trial design
Treatments tested in this trial
- Pacemaker - Physiological pacing
- Pacemaker - Right Ventricular pacing
Treatment groups
Sponsors and collaborators
Imperial College London
Lead sponsor
British Heart Foundation
Collaborator