Assessing treatment strategies for stroke patients with atrial fibrillation
Official title: Multimodal Prognostic Assessment of Acute Ischemic Stroke Patients With Atrial Fibrillation: a Prospective, Multicenter, Observational Study (IAT-CLOSURE)
Run by Jinan Central Hospital · NCT06548269 · Data updated 2026-11-12
This study is testing different treatment options for stroke patients with atrial fibrillation to see which one helps them recover better and prevents future strokes.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 1000 (estimated) |
| Sponsor | Jinan Central Hospital Academic / other |
| Locations | 1 site (Jinan, Shandong) |
| Status | Recruiting |
| Started | November 15, 2024 |
| Main results expected | May 31, 2027 |
| Study ends | May 31, 2029 |
| Registry record updated | May 22, 2025 |
| Trial ID | NCT06548269 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults over 18 years old who have experienced an acute ischemic stroke within the last 14 days and have been diagnosed with non-valvular atrial fibrillation.
✕Probably not a fit
Patients with pacemakers, implantable cardioverter defibrillators, or those who have had their left atrial appendage removed will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study investigates the safety and outcomes of various treatment strategies for patients with acute ischemic stroke and atrial fibrillation. It focuses on comparing best medical therapy, including oral anticoagulation and antiplatelet therapy, with left atrial appendage closure. The study employs a multimodal assessment approach, integrating brain and cardiologic evaluations to optimize secondary prevention of stroke. By utilizing prolonged cardiac monitoring, the study aims to improve detection rates of atrial fibrillation in stroke patients and assess the prognostic implications of AF burden.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment strategies and better outcomes for patients with acute ischemic stroke and atrial fibrillation.
How similar studies have gone: Other studies have shown success in using prolonged cardiac monitoring to detect atrial fibrillation in stroke patients, indicating that this approach has been validated in similar contexts.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Age \> 18 years old; 2. Acute ischemic stroke with onset ≤ 14 days; 3. Previously or during this hospitalization diagnosed with non-valvular atrial fibrillation; 4. Informed consent obtained from the patient or his/her legal representative; Exclusion Criteria: 1. Pacemaker, implantable cardioverter defibrillator or implantable cardiac monitor; 2. Left atrial appendage has been removed or post occlusion device implantation; 3. Transient AF secondary to other reversible disorders; 4. Life expectancy less than 1 year; 5. Patients that cannot complete subsequent follow-up (e.g. no fixed residence, overseas patients, etc.); 6. Females who are pregnant or in lactation; 7. Participating in other clinical trials that could confound the evaluation of the study; 8. Other circumstances that the investigator considers inappropriate for participation or may pose a significant risk to patients.
Where it's running
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Jinan Central Hospital
Jinan, Shandong, China Recruiting
Study contacts
- Study coordinator: Liqun Jiao
- Email: liqunjiao@sina.cn
- Phone: 13911224991
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.