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Systematic Ambulatory ECG Monitoring Following TAVI (RECORDII)

Systematic Ambulatory ECG Monitoring Following TAVI: A Prospective Randomized Trial.

This multicenter, prospective, randomized superiority trial will evaluate whether systematic 14-day ambulatory ECG monitoring following hospital discharge after transcatheter aortic valve implantation (TAVI) reduces the risk of sudden death, symptomatic arrhythmic events, or stroke within 1 year compared with standard post-discharge care. Patients undergoing successful TAVI without permanent pacemaker implantation and presenting with at least one ECG conduction abnormality at hospital discharge will be randomized to receive either ambulatory ECG monitoring or standard follow-up. All participants will undergo routine clinical follow-up at 30 days and 1 year after TAVI.

Visão geral do estudo

Status

Ainda não está recrutando

Intervenção / Tratamento

Descrição detalhada

Transcatheter aortic valve implantation (TAVI) is an established treatment for severe aortic stenosis. Despite advances in transcatheter heart valve technology and procedural techniques, conduction disturbances remain among the most frequent complications following TAVI. High-grade atrioventricular block, complete heart block, and new-onset bundle branch block may occur after the procedure and can lead to delayed permanent pacemaker implantation or life-threatening arrhythmic events. The increasing adoption of minimalist TAVI pathways with hospital discharge within 24-72 hours raises concerns that clinically significant arrhythmias may develop after discharge and remain undetected.

Ambulatory electrocardiographic (ECG) monitoring provides continuous rhythm surveillance during daily activities and enables the early detection of both symptomatic and asymptomatic bradyarrhythmias and tachyarrhythmias. Previous observational studies have demonstrated that clinically significant bradyarrhythmias occur in approximately 5-10% of patients during the first weeks after TAVI, particularly among those with baseline or new-onset conduction abnormalities. Ambulatory ECG monitoring has also identified previously unrecognized atrial fibrillation, allowing timely initiation of anticoagulation therapy in patients at high risk of thromboembolic events.

Although several prospective studies have evaluated ambulatory ECG monitoring after TAVI, most have been observational and were designed primarily to describe the incidence of post-procedural arrhythmias rather than to assess their impact on clinical outcomes. Preliminary evidence from the RECORD pilot study suggested that systematic ambulatory ECG monitoring after hospital discharge was associated with earlier identification and treatment of clinically significant arrhythmias and a reduction in the composite of sudden death, symptomatic arrhythmic events, and stroke during 1-year follow-up, with the greatest benefit observed among patients with conduction abnormalities at hospital discharge.

This randomized trial has been designed to provide definitive evidence regarding the clinical value of systematic ambulatory ECG monitoring after TAVI in patients at increased risk of post-procedural conduction disturbances. The study will evaluate whether early detection and management of clinically significant arrhythmias can improve clinical outcomes during the year following the procedure.

Tipo de estudo

Intervencional

Inscrição (Estimado)

754

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

Locais de estudo

    • Quebec
      • Québec, Quebec, Canadá, G1Y 4G5
        • Institut universitaire de cardiologie et de pneumologie de Québec - UL
        • Contato:
        • Investigador principal:
          • Josep Rodés-Cabau, MD, PhD
        • Subinvestigador:
          • Francois Philippon, MD

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  • Age >18 years
  • Successful TAVI procedure.
  • Hospitalization discharge ≤72 hrs following the TAVI procedure.
  • Presence of at least 1 ECG abnormality at hospital discharge (QRS ≥120 ms OR PR ≥200 ms)

Exclusion Criteria:

  • Pacemaker implantation (pre- TAVI or during hospitalization after the procedure).
  • TAVI valve-in-valve procedure
  • Any complication or logistic reason precluding hospital discharge ≤72 hrs following the TAVI procedure.
  • Impossibility to obtain signed informed consent.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Ambulatory ECG monitoring
Participants will undergo ambulatory ECG monitoring at hospital discharge following TAVI. Continuous ECG monitoring will be performed for 14 days using an ambulatory ECG monitoring device. Clinically significant bradyarrhythmias or tachyarrhythmias detected during monitoring will be reviewed and managed according to clinical practice, including appropriate therapeutic interventions when indicated.
Participants randomized to the intervention arm will undergo systematic ambulatory ECG monitoring at hospital discharge following the TAVI procedure. A wearable ambulatory ECG monitoring device will be applied for continuous rhythm monitoring during a 14-day period. The device will allow detection of clinically significant bradyarrhythmias and tachyarrhythmias. Detected arrhythmic events will be reviewed by the study team, and appropriate clinical management, including further evaluation or therapeutic intervention, will be performed according to the nature of the detected abnormality and standard clinical practice.
Sem intervenção: Standard care (no ambulatory ECG monitoring device).
Participants will receive standard post-TAVI care without systematic ambulatory ECG monitoring at hospital discharge. Clinical follow-up will be performed according to routine practice.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Rate of the combined endpoint (sudden death, symptomatic arrhythmias or stroke)
Prazo: Within the year following the TAVI procedure
Composite endpoint including sudden death, symptomatic arrhythmias, or stroke.
Within the year following the TAVI procedure

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Incidence of sudden death
Prazo: 1 year after TAVI
Sudden death
1 year after TAVI
Incidence of symptomatic arrhythmias
Prazo: 1 year after TAVI
All symptomatic arrhythmias events
1 year after TAVI
Incidence of stroke
Prazo: 1 year after TAVI
All stroke events
1 year after TAVI
Incidence of PPI
Prazo: 30 days after TAVI
Number of patients with PPI
30 days after TAVI
Incidence of PPI
Prazo: 1 year after TAVI
Number of patients with PPI
1 year after TAVI
Incidence of the combined endpoint (sudden death, symptomatic arrhythmias or stroke) at 30 days
Prazo: 30 days after TAVI
Composite endpoint including sudden death, symptomatic arrhythmias, or stroke.
30 days after TAVI
Incidence of sudden death
Prazo: 30 days after TAVI
Sudden death
30 days after TAVI
Incidence of symptomatic arrhytmias
Prazo: 30 days after TAVI
All symptomatic arrhythmias events
30 days after TAVI
Incidence of stroke
Prazo: 30 days after TAVI
All stroke events
30 days after TAVI
Incidence of the combined endpoint (sudden death, symptomatic arrhythmias, stroke) according to patient sex
Prazo: 1 year after TAVI
Composite endpoint including sudden death, symptomatic arrhythmias, or stroke, analyzed according to patient sex.
1 year after TAVI
Incidence of the combined endpoint of sudden death, symptomatic arrhythmias, or stroke) according to ECG abnormalities
Prazo: 1 year after TAVI
Composite endpoint including sudden death, symptomatic arrhythmias, or stroke, analyzed according to ECG abnormality status (pre-existing versus new-onset after TAVI).
1 year after TAVI
Incidence of the combined endpoint according to baseline ECG abnormality type
Prazo: 1 year after TAVI
Composite endpoint (sudden death, symptomatic arrhythmias, or stroke) analyzed according to the type of ECG abnormality present before TAVI.
1 year after TAVI
Incidence of sudden death according to baseline ECG abnormality type
Prazo: 1 year after TAVI
Sudden death analyzed according to the type of ECG abnormality present before TAVI.
1 year after TAVI
Incidence of symptomatic arrhythmias according to baseline ECG abnormality type
Prazo: 1 year after TAVI
Symptomatic arrhythmias according to the type of ECG abnormality present before TAVI.
1 year after TAVI
Incidence of stroke according to baseline ECG abnormality type
Prazo: 1 year after TAVI
Stroke according to the type of ECG abnormality present before TAVI.
1 year after TAVI
Incidence of the combined endpoint according to discharge ECG abnormality type
Prazo: 1 year after TAVI
Composite endpoint (sudden death, symptomatic arrhythmias, or stroke) according to the type of ECG abnormality present at hospital discharge.
1 year after TAVI
Incidence of sudden death according to discharge ECG abnormality type
Prazo: 1 year after TAVI
Sudden death according to the type of ECG abnormality present at hospital discharge.
1 year after TAVI
Incidence of symptomatic arrhythmias according to discharge ECG abnormality type
Prazo: 1 year after TAVI
Symptomatic arrhythmias according to the type of ECG abnormality present at hospital discharge.
1 year after TAVI
Incidence of stroke according to discharge ECG abnormality type
Prazo: 1 year after TAVI
Stroke according to the type of ECG abnormality present at hospital discharge.
1 year after TAVI
Change in quality of life
Prazo: Baseline to 1 year after TAVI
Quality of life assessed using the EQ-5D-5L questionnaire.
Baseline to 1 year after TAVI
Percentage of ventricular pacing
Prazo: 1 year after TAVI
Ventricular pacing burden in participants with permanent pacemakers.
1 year after TAVI
Incidence of all-cause mortality
Prazo: 30 days after TAVI
All-cause mortality
30 days after TAVI
Incidence of cardiovascular mortality
Prazo: 30 days after TAVI
Cardiovascular mortality
30 days after TAVI
Incidence of all-cause mortality
Prazo: 1 year after TAVI
All cause mortality
1 year after TAVI
Incidence of cardiovasculare mortality
Prazo: 1 year after TAVI
Cardiovascular mortality
1 year after TAVI

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: Josep Rodes-Cabau, MSc, Fondation IUCPQ

Publicações e links úteis

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Publicações Gerais

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de agosto de 2026

Conclusão Primária (Estimado)

1 de dezembro de 2028

Conclusão do estudo (Estimado)

1 de dezembro de 2028

Datas de inscrição no estudo

Enviado pela primeira vez

21 de julho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

27 de julho de 2026

Primeira postagem (Real)

31 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

31 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

27 de julho de 2026

Última verificação

1 de julho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Descrição do plano IPD

A decision regarding IPD sharing has not yet been made. Following study completion, requests for access to de-identified individual participant data may be considered by the sponsor on a case-by-case basis, subject to ethical, legal, and institutional requirements.

Informações sobre medicamentos e dispositivos, documentos de estudo

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Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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