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Recruiting NCT07278089

NCT07278089 AF Screening in Patients With Abnormal Echocardiographic Parameters

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Clinical Trial Summary
NCT ID NCT07278089
Status Recruiting
Phase
Sponsor Tze-Fan Chao
Condition Atrial Fibrillation (AF)
Study Type INTERVENTIONAL
Enrollment 3,000 participants
Start Date 2025-03-17
Primary Completion 2031-12-31

Eligibility & Interventions

Sex All sexes
Min Age 20 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
study arm

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 3,000 participants in total. It began in 2025-03-17 with a primary completion date of 2031-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

To evaluate the feasibility of specific echocardiographic parameters as criteria for AF screening and to determine the AF detection yield of scheduled extended ECG monitoring compared to contemporary care.

Eligibility Criteria

Inclusion Criteria: patients who met any of the following criteria 1. LAE: defined as LAD ≥ 45 mm or LAVI \> 34 ml/m2; 2. LVH: defined as LV septal or posterior wall thickness ≥ 15 mm; 3. E/e' \> 14; 4. grade II or III diastolic dysfunction; 5. VHD; 6. HF: defined as LVEF \< 40% or LVEF ≥40% with clinical presentation compatible with Framingham criteria, New York Heart Association functional classification II-IV, and N-terminal pro-B type natriuretic peptide (NT-proBNP) \> 125 pg/ml. Exclusion Criteria: * Patients with a history of AF or atrial flutter, congenital heart disease, acute coronary syndrome undergoing urgent percutaneous coronary intervention within 3 months, uncontrolled hyperthyroidism, end-stage renal disease, unstable hemodynamic status or any known major comorbidities or medical conditions with expected life expectancy less than 1 year are excluded.

Contact & Investigator

Central Contact

Tze-Fan Chao, PhD

✉ eyckeyck@gmail.com

📞 886-2-28727794

Frequently Asked Questions

Who can join the NCT07278089 clinical trial?

This trial is open to participants of all sexes, aged 20 Years or older, studying Atrial Fibrillation (AF). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07278089 currently recruiting?

Yes, NCT07278089 is actively recruiting participants. Contact the research team at eyckeyck@gmail.com for enrollment information.

Where is the NCT07278089 trial being conducted?

This trial is being conducted at Taipei, Taiwan.

Who is sponsoring the NCT07278089 clinical trial?

NCT07278089 is sponsored by Tze-Fan Chao. The trial plans to enroll 3,000 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology