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Progressive ablation of persistent atrial fibrillation with nifekaran intervention

Safety and efficacy of progressive ablation of persistent atrial fibrillation with nifekaran intervention: a prospective, single-center clinical trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054521
Enrollment
Unknown
Registered
2021-12-19
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-11-28

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

Conditions

Persistent atrial fibrillation

Interventions

Experimental group:Nifekaran intravenous infusion (0.4mg/kg)
Control Group:electrical cardioversion

Sponsors

The Second Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 80 years, gender is not limited; 2. Patients with persistent atrial fibrillation confirmed by electrocardiogram; 3. Those who intend to undergo catheter ablation of atrial fibrillation; 4. Those who agree to participate in this study and voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients who have received atrial fibrillation catheter radiofrequency ablation in the past; 2. Left atrial thrombus (confirmed by esophageal ultrasonography) or left atrial diameter >=55mm; 3. Patients with thrombocytopenia (PLT= 3 times the upper limit of normal; serum creatinine > 3.5 mg/dl); 6. Patients with abnormal thyroid function; 7. Patients with a history of surgery in the past 3 months; 8. Patients with organic diseases such as stroke, kidney damage, malignant tumor, liver and pulmonary fibrosis; 9. Life expectancy < 12 months.

Design outcomes

Primary

MeasureTime frame
Atrial fibrillation recurred 6 months later;

Countries

China

Contacts

Public ContactXia Zirong

The Second Affiliated Hospital of Nanchang University

425599293@qq.com+86 18770065677

Outcome results

None listed

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