このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

Effect of Tirzepatide on Recurrence of Atrial Fibrillation After Catheter Ablation in Obese Patients (TEAR-AF)

2026年7月15日 更新者:Yunlong Wang

Effect of Tirzepatide on Recurrence of Atrial Fibrillation After Catheter Ablation in Obese Patients: A Multicenter, Randomized, Open-Label Trial

Obese patients with atrial fibrillation (AF) have a high recurrence rate after catheter ablation, even at experienced centers. Weight reduction improves post-ablation outcomes, but lifestyle measures alone are difficult to sustain. Tirzepatide, a once-weekly GIP/GLP-1 dual receptor agonist, produces greater weight loss than GLP-1 monotherapy and may confer additional cardiometabolic benefits. This multicenter, randomized, open-label, parallel-group, superiority trial evaluates whether adding standardized tirzepatide treatment to a structured lifestyle intervention - compared with the lifestyle intervention alone - reduces AF recurrence within 1 year after ablation in obese patients.

調査の概要

詳細な説明

Eligible obese patients (or overweight patients with a weight-related comorbidity) with symptomatic paroxysmal or persistent AF undergoing catheter ablation will be screened within 28 days before the procedure. After ablation with restoration of sinus rhythm, participants will be randomized 1:1 to (a) tirzepatide plus standardized lifestyle intervention and standard AF management, or (b) standardized lifestyle intervention and standard AF management alone. Randomization is stratified by study center, AF type (paroxysmal/persistent), baseline BMI, and diabetes status.

A 90-day post-ablation blanking period (Day 0-90) is excluded from the primary efficacy assessment. The primary efficacy assessment window runs from Day 91 to Day 365. Tirzepatide is administered subcutaneously once weekly and titrated per the China NMPA label using an individualized dose-adjustment SOP, continuing through Week 52. Both groups receive guideline-directed periprocedural anticoagulation, standardized antiarrhythmic drug (AAD) use, an individualized exercise prescription, a modified Mediterranean diet (target intake = total energy expenditure - 500 kcal), and management of smoking, alcohol, comorbidities, sleep, and obstructive sleep apnea (OSA).

Approximately 8-12 tertiary (Class 3A) hospitals in China with mature AF ablation teams will participate. Planned enrollment is 710 participants.

研究の種類

介入

入学 (推定)

710

段階

  • フェーズ 4

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 and ≤75 years at the time of screening
  • Documented symptomatic paroxysmal AF or persistent AF, confirmed by 12-lead ECG, Holter monitoring, or cardiac monitoring device, with documented AF episode duration ≥7 days (for persistent AF) and total AF history duration ≤5 years
  • Body weight criteria (aligned with NMPA-approved tirzepatide indication) meeting at least one of the following:

BMI ≥28.0 kg/m² (obesity threshold per Chinese criteria), OR BMI ≥24.0 kg/m² and <28.0 kg/m² (overweight per Chinese criteria) with at least one weight-related comorbidity: hypertension, dyslipidemia, type 2 diabetes mellitus (T2DM), obstructive sleep apnea syndrome (OSAS), or atherosclerotic cardiovascular disease (ASCVD)

  • Failed response to or intolerance of at least one antiarrhythmic drug (AAD), or explicit patient preference for a rhythm control strategy
  • Undergoing catheter ablation for AF at a participating center, with confirmed successful restoration of sinus rhythm at the end of the procedure (as determined by the operator)
  • Willing and able to understand the study procedures, provide written informed consent, and comply with all protocol requirements including 12-month follow-up visits
  • Capable of performing basic physical activity (no absolute contraindication to moderate-intensity aerobic exercise)

Exclusion Criteria:

Cardiovascular Exclusion Criteria

  • Long-standing persistent AF: continuous AF duration ≥5 years prior to enrollment
  • Prior catheter ablation for AF or atrial flutter at any time
  • Left atrial anteroposterior diameter >55 mm (by transthoracic echocardiography at screening)
  • Left ventricular ejection fraction (LVEF) <35% at screening
  • NYHA functional class III or IV heart failure
  • Significant structural heart disease: hypertrophic cardiomyopathy, valvular heart disease requiring intervention, congenital heart disease, myocarditis, or cardiac sarcoidosis
  • Acute coronary syndrome (ACS), ischemic stroke/TIA, or major cardiac surgery within 6 months prior to screening

Tirzepatide-Specific Exclusion Criteria (per NMPA Prescribing Information)

  • Prior use of any GLP-1 receptor agonist (liraglutide, semaglutide, dulaglutide, exenatide, etc.) or GIP receptor agonist, or known hypersensitivity to tirzepatide or any excipient in the formulation
  • Personal or family (first-degree relative) history of multiple endocrine neoplasia type 2 (MEN2) or medullary thyroid carcinoma (MTC)
  • History of acute pancreatitis or chronic pancreatitis, or current symptomatic cholelithiasis or cholecystitis
  • Type 1 DM
  • Severe gastrointestinal disease including severe gastroparesis, inflammatory bowel disease, or any condition that would substantially impair gastrointestinal motility or absorption

General Exclusion Criteria

  • Use of any weight-loss medication (orlistat, phentermine, naltrexone/bupropion, or other anti-obesity agents) or participation in any weight-loss pharmacotherapy clinical trial within 3 months prior to screening
  • Severe hepatic insufficiency (Child-Pugh class C) or severe renal insufficiency (eGFR <15 mL/min/1.73 m²)
  • Active malignancy (receiving systemic anti-cancer treatment or with life expectancy <2 years due to malignancy)
  • Pregnancy, breastfeeding, or women of childbearing potential who are unwilling to use highly effective contraception throughout the study and for ≥1 month after the last dose of tirzepatide
  • Severe psychiatric disorder (schizophrenia, bipolar disorder, severe major depressive disorder) that would impair ability to comply with study procedures
  • Known allergy or sensitivity to adhesive patch materials (relevant to ECG monitoring patch components)
  • Any other condition that, in the opinion of the investigator, would make participation inadvisable or compromise the safety of the participant or the integrity of the study

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:独身

武器と介入

参加者グループ / アーム
介入・治療
実験的:Tirzepatide + Lifestyle Intervention

Standardized lifestyle intervention and standard AF management plus once-weekly subcutaneous tirzepatide, initiated after randomization and continued through Week 52.

Tirzepatide titration (per NMPA label):

  • Weeks 1-4: 2.5 mg once weekly (initiation)
  • Weeks 5-16: escalate by 2.5 mg every 4 weeks (5 mg → 7.5 mg → 10 mg)
  • Weeks 17-52: maintenance 10 mg once weekly, up-titratable to 15 mg (maximum dose 15 mg)

Dual GIP and GLP-1 receptor agonist administered as a weekly subcutaneous injection.

Titrated from 2.5 mg/week to a target of 10 mg/week over 12 weeks, then maintained at the maximum tolerated dose for the remainder of the 52-week treatment period.

他の名前:
  • ムンジャロ

Guideline-directed AF management (rate/rhythm control, anticoagulation by CHA2DS2-VASc).

Structured lifestyle intervention: 500 kcal/day caloric deficit; exercise prescription of ≥150 min/week moderate aerobic; smoking cessation and alcohol moderation counseling.

アクティブコンパレータ:Lifestyle Intervention

AF Management and Post-Ablation Care

  • Ablation technique: circumferential pulmonary vein isolation (CPVI) ± adjunctive linear ablation at operator discretion, using established mapping and energy delivery protocols
  • Peri-procedural anticoagulation: guideline-directed anticoagulation
  • Antiarrhythmic drug (AAD) use: standardized per protocol SOP;

Exercise Intervention • Target: moderate-intensity aerobic exercise ≥150 minutes per week, OR vigorous-intensity aerobic exercise ≥75 minutes per week

Dietary Intervention

• Caloric target: estimated total energy expenditure (TEE) minus 500 kcal/day

Other Risk Factor Management

  • Smoking cessation
  • Alcohol restriction
  • Comorbidity management
  • OSA management

Guideline-directed AF management (rate/rhythm control, anticoagulation by CHA2DS2-VASc).

Structured lifestyle intervention: 500 kcal/day caloric deficit; exercise prescription of ≥150 min/week moderate aerobic; smoking cessation and alcohol moderation counseling.

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
Number of Participants With Recurrence of Atrial Fibrillation, Atrial Flutter, or Atrial Tachycardia
時間枠:Day 91 through Week 52 after catheter ablation
Any documented atrial arrhythmia - defined as AF, atrial flutter (AFL), or atrial tachycardia (AT) - lasting ≥30 seconds, in the absence of antiarrhythmic drug (AAD) use.
Day 91 through Week 52 after catheter ablation

二次結果の測定

結果測定
メジャーの説明
時間枠
Time to Death From Any Cause
時間枠:Day 1 through Week 52
Time to death from any cause.
Day 1 through Week 52
Percentage of Monitoring Time Spent in Atrial Fibrillation (AF Burden)
時間枠:At Week 12, Week 26, and Week 52
Percentage of total monitoring time spent in AF, measured by 7-day ambulatory ECG patch.
At Week 12, Week 26, and Week 52
Change in body weight
時間枠:Baseline to Week 52
Absolute and percentage change in body weight from baseline to baseline to 52 weeks.
Baseline to Week 52
Change in BMI
時間枠:Baseline to Week 52
Change from baseline to 52 weeks in body mass index (kg/m²)
Baseline to Week 52
Change in waist circumference
時間枠:Baseline to Week 52
Change from baseline to 52 weeks waist circumference (cm).
Baseline to Week 52
Change in left atrial volume index (LAVI)
時間枠:Baseline to Week 52
Change in echocardiographic LAVI (mL/m²) from baseline to 52 weeks measured by core laboratory.
Baseline to Week 52
Change in N-terminal pro-B-type natriuretic peptide (NT-proBNP)
時間枠:Baseline to Week 52
Change in serum NT-proBNP concentration from baseline to 52 weeks, measured by central laboratory.
Baseline to Week 52
Change in Serum High-Sensitivity C-Reactive Protein (hs-CRP) Concentration
時間枠:Baseline to Week 52
Change in serum high-sensitivity C-reactive protein (hs-CRP) concentration from baseline to 52 weeks, measured by central laboratory.
Baseline to Week 52
Time to Cardiovascular Death
時間枠:Day 1 through Week 52
Time to cardiovascular death.
Day 1 through Week 52

その他の成果指標

結果測定
メジャーの説明
時間枠
Change in epicardial adipose tissue volume
時間枠:Baseline to Week 52
Change in epicardial adipose tissue volume measured by cardiac CT from baseline to 12 months.
Baseline to Week 52

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。

スポンサー

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9月1日

一次修了 (推定)

2029年9月1日

研究の完了 (推定)

2029年12月30日

試験登録日

最初に提出

2026年7月15日

QC基準を満たした最初の提出物

2026年7月15日

最初の投稿 (実際)

2026年7月21日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月21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15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?

はい

IPD プランの説明

Individual de-identified participant data underlying the published results, together with the study protocol, statistical analysis plan, and data dictionary, will be made available upon reasonable request after publication of the primary results.

IPD 共有時間枠

Beginning 12 months after publication of the primary results, ending 5 years thereafter.

IPD 共有アクセス基準

Requests reviewed by the trial steering committee. Investigators must submit a methodologically sound proposal, have approval from an independent review committee, and sign a data use agreement.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

購読する