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Study on the correlation between polymorphism of drug metabolism enzymes and transporters genes and the pharmacokinetics of rivaroxaban, efficacy, and safety in patients after radiofrequency ablation for atrial fibrillation.

Study on the correlation between polymorphism of drug metabolism enzymes and transporters genes and the pharmacokinetics of rivaroxaban, efficacy, and safety in patients after radiofrequency ablation for atrial fibrillation.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500095918
Enrollment
Unknown
Registered
2025-01-15
Start date
2023-04-07
Completion date
Unknown
Last updated
2025-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Patients with atrial fibrillation who have undergone radiofrequency ablation surgery and are receiving anticoagulation therapy with rivaroxaban.:NA

Sponsors

Huzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years, gender not specified; 2. Meet the diagnostic criteria for non-valvular atrial fibrillation according to the 2020 European Society of Cardiology (ESC) guidelines, which include a standard 12-lead ECG recording or a single-lead ECG recording of at least 30 seconds with the disappearance of P waves and irregular RR intervals (without impaired atrioventricular conduction), and have clinical symptoms, and are stable patients receiving radiofrequency ablation for atrial fibrillation and taking rivaroxaban 15 or 20 mg (once a day, qd) anticoagulation therapy at our hospital; 3. After being fully informed, voluntarily sign the clinical biological sample collection informed consent form of our hospital.

Exclusion criteria

Exclusion criteria: 1. Patients who are taking any other anticoagulant drugs or who are using ketoconazole, cyclosporine, etc., which interfere with the metabolism of rivaroxaban; 2. Patients who do not adhere to the treatment regimen; 3. Patients who do not undergo follow-up checks at our hospital at the specified time during their treatment; 4 .Patients who are unable or unwilling to cooperate with the collection of clinical information (e.g., patients with mental disorders, memory disorders, etc.); 5. Patients who, in the judgment of the research team, have other conditions that are not appropriate for participation in this study.

Design outcomes

Primary

MeasureTime frame
plasma concentration;Gene polymorphism;Laboratory indicators;concomitant medication;

Secondary

MeasureTime frame
Basic information of patients;

Countries

China

Contacts

Public ContactGu Fangfang

Huzhou Central Hospital

390904165@qq.com+86 137 5421 7729

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026