- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07715929
Effect of Tirzepatide on Recurrence of Atrial Fibrillation After Catheter Ablation in Obese Patients (TEAR-AF)
Effect of Tirzepatide on Recurrence of Atrial Fibrillation After Catheter Ablation in Obese Patients: A Multicenter, Randomized, Open-Label Trial
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Einschreibung (Geschätzt)
Phase
- Phase 4
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
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):
|
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.
Andere Namen:
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. |
|
Aktiver Komparator: Lifestyle Intervention
AF Management and Post-Ablation Care
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
|
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. |
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Number of Participants With Recurrence of Atrial Fibrillation, Atrial Flutter, or Atrial Tachycardia
Zeitfenster: 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
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Time to Death From Any Cause
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: Baseline to Week 52
|
Change from baseline to 52 weeks in body mass index (kg/m²)
|
Baseline to Week 52
|
|
Change in waist circumference
Zeitfenster: Baseline to Week 52
|
Change from baseline to 52 weeks waist circumference (cm).
|
Baseline to Week 52
|
|
Change in left atrial volume index (LAVI)
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: Day 1 through Week 52
|
Time to cardiovascular death.
|
Day 1 through Week 52
|
Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Change in epicardial adipose tissue volume
Zeitfenster: Baseline to Week 52
|
Change in epicardial adipose tissue volume measured by cardiac CT from baseline to 12 months.
|
Baseline to Week 52
|
Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Herz-Kreislauf-Erkrankungen
- Pathologische Prozesse
- Ernährungsstörungen
- Herzkrankheiten
- Überernährung
- Körpergewicht
- Arrhythmien, Herz
- Pathologische Zustände, Anzeichen und Symptome
- Ernährungs- und Stoffwechselerkrankungen
- Anzeichen und Symptome
- Übergewicht
- Fettleibigkeit
- Vorhofflimmern
- Aminosäuren, Peptide und Proteine
- Proteine
- Glucagon-ähnliches Peptid-1-Rezeptor
- Glucagon-ähnliche Peptidrezeptoren
- Rezeptoren, G-Protein-gekoppelt
- Rezeptoren, Zelloberfläche
- Membranproteine
- Rezeptoren, Magen -Darm -Hormon
- Rezeptoren, Peptid
- Tirzepatid
Andere Studien-ID-Nummern
- TEAR-AF-01
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Beschreibung des IPD-Plans
IPD-Sharing-Zeitrahmen
IPD-Sharing-Zugriffskriterien
Art der unterstützenden IPD-Freigabeinformationen
- STUDIENPROTOKOLL
- SAFT
- ICF
- CSR
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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