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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.

調査の概要

状態

まだ募集していません

詳細な説明

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.

研究の種類

介入

入学 (推定)

754

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

    • Quebec
      • Québec、Quebec、カナダ、G1Y 4G5
        • Institut universitaire de cardiologie et de pneumologie de Québec - UL
        • コンタクト:
        • 主任研究者:
          • Josep Rodés-Cabau, MD, PhD
        • 副調査官:
          • Francois Philippon, MD

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.
介入なし: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Rate of the combined endpoint (sudden death, symptomatic arrhythmias or stroke)
時間枠:Within the year following the TAVI procedure
Composite endpoint including sudden death, symptomatic arrhythmias, or stroke.
Within the year following the TAVI procedure

二次結果の測定

結果測定
メジャーの説明
時間枠
Incidence of sudden death
時間枠:1 year after TAVI
Sudden death
1 year after TAVI
Incidence of symptomatic arrhythmias
時間枠:1 year after TAVI
All symptomatic arrhythmias events
1 year after TAVI
Incidence of stroke
時間枠:1 year after TAVI
All stroke events
1 year after TAVI
Incidence of PPI
時間枠:30 days after TAVI
Number of patients with PPI
30 days after TAVI
Incidence of PPI
時間枠: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
時間枠:30 days after TAVI
Composite endpoint including sudden death, symptomatic arrhythmias, or stroke.
30 days after TAVI
Incidence of sudden death
時間枠:30 days after TAVI
Sudden death
30 days after TAVI
Incidence of symptomatic arrhytmias
時間枠:30 days after TAVI
All symptomatic arrhythmias events
30 days after TAVI
Incidence of stroke
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠:1 year after TAVI
Ventricular pacing burden in participants with permanent pacemakers.
1 year after TAVI
Incidence of all-cause mortality
時間枠:30 days after TAVI
All-cause mortality
30 days after TAVI
Incidence of cardiovascular mortality
時間枠:30 days after TAVI
Cardiovascular mortality
30 days after TAVI
Incidence of all-cause mortality
時間枠:1 year after TAVI
All cause mortality
1 year after TAVI
Incidence of cardiovasculare mortality
時間枠:1 year after TAVI
Cardiovascular mortality
1 year after TAVI

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Josep Rodes-Cabau, MSc、Fondation IUCPQ

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

一般刊行物

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年8月1日

一次修了 (推定)

2028年12月1日

研究の完了 (推定)

2028年12月1日

試験登録日

最初に提出

2026年7月21日

QC基準を満たした最初の提出物

2026年7月27日

最初の投稿 (実際)

2026年7月31日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月31日

QC基準を満たした最後の更新が送信されました

2026年7月27日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

未定

IPD プランの説明

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.

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