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

15 de julio de 2026 actualizado por: 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.

Descripción general del estudio

Estado

Aún no reclutando

Condiciones

Intervención / Tratamiento

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

710

Fase

  • Fase 4

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

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

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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.

Otros nombres:
  • Monjaro

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.

Comparador activo: 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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Number of Participants With Recurrence of Atrial Fibrillation, Atrial Flutter, or Atrial Tachycardia
Periodo de tiempo: 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

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Time to Death From Any Cause
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: Baseline to Week 52
Change from baseline to 52 weeks in body mass index (kg/m²)
Baseline to Week 52
Change in waist circumference
Periodo de tiempo: Baseline to Week 52
Change from baseline to 52 weeks waist circumference (cm).
Baseline to Week 52
Change in left atrial volume index (LAVI)
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: Day 1 through Week 52
Time to cardiovascular death.
Day 1 through Week 52

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in epicardial adipose tissue volume
Periodo de tiempo: Baseline to Week 52
Change in epicardial adipose tissue volume measured by cardiac CT from baseline to 12 months.
Baseline to Week 52

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de septiembre de 2026

Finalización primaria (Estimado)

1 de septiembre de 2029

Finalización del estudio (Estimado)

30 de diciembre de 2029

Fechas de registro del estudio

Enviado por primera vez

15 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

15 de julio de 2026

Publicado por primera vez (Actual)

21 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

21 de julio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

15 de julio de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • TEAR-AF-01

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Descripción del plan IPD

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.

Marco de tiempo para compartir IPD

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

Criterios de acceso compartido de IPD

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.

Tipo de información de apoyo para compartir IPD

  • PROTOCOLO DE ESTUDIO
  • SAVIA
  • CIF
  • RSC

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .