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Construction of a cohort of elderly atrial fibrillation patients at high risk of stroke and its intelligent management

Construction of a cohort of elderly atrial fibrillation patients at high risk of stroke and its intelligent management

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125579
Enrollment
Unknown
Registered
2026-05-28
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

atrial fibrillation

Interventions

Observation group:None

Sponsors

Shanghai East Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 65 years; 2. Diagnosed with atrial fibrillation, with the diagnosis based on but not limited to 12-lead electrocardiogram, Holter monitoring, or other cardiac rhythm monitoring devices. 3. CHA2DS2-VA score >= 2 (according to the Chinese Atrial Fibrillation Management Guidelines (2025), a score >= 2 indicates high risk of stroke and anticoagulant medications should be used). 4. Willing and able to provide written informed consent; 5. Willing and able to cooperate with completing baseline surveys and regular follow-ups;

Exclusion criteria

Exclusion criteria: 1.History of uncontrolled serious ventricular arrhythmias (e.g., ventricular tachycardia, ventricular fibrillation). 2.Severe mental disorders that prevent cooperation with the study. 3.Other reasons deemed by the investigator as making the participant unsuitable for this study. 4.The participant or their family members refuse to cooperate with follow-up.

Design outcomes

Primary

MeasureTime frame
Major Adverse Cardiovascular and Cerebrovascular Events (MACE);

Secondary

MeasureTime frame
Incidence of individual endpoint events among the primary outcome variables;

Countries

China

Contacts

Public ContactXiaorong Li

Shanghai East Hospital

jsxrli@yeah.net+86 21 5065 1851

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026