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A Study on the Correlation Between Periodontitis and Its Treatment and Recurrence After Catheter Ablation for Atrial Fibrillation

A Study on the Correlation Between Periodontitis and Its Treatment and Recurrence After Catheter Ablation for Atrial Fibrillation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129419
Enrollment
Unknown
Registered
2026-08-04
Start date
2026-08-10
Completion date
Unknown
Last updated
2026-08-10

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

Conditions

Atrial fibrillation, moderate to severe periodontitis

Interventions

Non-periodontitis group:None
Group with periodontitis who haven't received periodontal treatment:None
Periodontitis patients receiving basic periodontal treatment:None

Sponsors

Peking University Hospital of Stomatology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age: =18 years old; 2.Diagnosed with atrial fibrillation; 3.Planned for first catheter ablation; 4.At least 10 natural teeth; 5.No systematic periodontal treatment received in the past; 6.No smoking habit or smoking less than 10 cigarettes per day; 7.Subject informed consent.

Exclusion criteria

Exclusion criteria: 1.History of atrial fibrillation ablation or cardiac surgery; valvular heart disease (moderate to severe mitral or aortic valve lesions) or post-mechanical valve replacement; left atrial thrombus; severe heart failure (NYHA Class IV) or left ventricular ejection fraction 3 times the upper limit of normal, eGFR < 30ml/min); 6.Women who are pregnant, planning to become pregnant, or breastfeeding; 7.Patients who require long-term or intermittent antibiotic use and receive drug treatments known to affect periodontal conditions (such as amoxicillin); 8.Use of any systemic or topical immunosuppressants within the past 6 months; 9.At least one of the following conditions occurs: acute oral infection, acute oral pain (including pulpitis), suspicious oral mucosal lesions, severe oral inflammation unrelated to periodontal disease, or ongoing orthodontic treatment; 10.Participate in other clinical trials related to drugs or medical devices at the same time; 11.Subjects with severe difficulties in comprehending written and spoken grammar; 12.Persons with other circumstances that may affect the conduct of this study.

Design outcomes

Primary

MeasureTime frame
Periodontal related indicators;Baseline clinical data;Atrial fibrillation-related outcome indicators;Biological Sample Testing Indicators;

Countries

China

Contacts

Public ContactJiang Shengjie

Peking University Hospital of Stomatology

277062365@qq.com+86 10 6217 3403

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026