Comprehensive clinical rule to diagnose acute heart failure in the emergency department
Official title: Establishing a Comprehensive Clinical Prediction Rule for the Diagnosis of Acute Heart Failure in the Emergency Department
Run by Chinese University of Hong Kong · NCT07754084 · Data updated 2026-11-12
A prospective study tests a combined clinical rule using patient data, a point-of-care NT-proBNP test, an 8-point lung ultrasound, and bedside echo to quickly diagnose acute heart failure in adults with new or worsening symptoms.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 560 (estimated) |
| Sponsor | Chinese University of Hong Kong Academic / other |
| Locations | 3 sites (Hong Kong and 2 other locations) |
| Status | Recruiting |
| Started | August 17, 2026 |
| Main results expected | December 31, 2028 |
| Study ends | January 31, 2029 |
| Registry record updated | November 5, 2026 |
| Trial ID | NCT07754084 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 years and older with suspected acute heart failure or acute dyspnea.
✕Probably not a fit
Patients without acute heart failure or those not fitting the diagnostic pathway may not benefit from the rule.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This prospective observational study aims to develop a comprehensive prediction rule for diagnosing acute heart failure in the emergency department. It combines traditional clinical characteristics with point-of-care NT-proBNP testing, an 8-point lung ultrasound score, and rapid bedside echocardiography. The primary outcome is a validated diagnosis of acute heart failure, with secondary outcomes including ED and discharge diagnoses. The goal is to reduce diagnostic delays and improve accuracy to minimize potential harm to patients. The study is led by The Chinese University of Hong Kong with several collaborating hospitals in Hong Kong.
Why it matters
Potential benefit: If successful, the rule could speed up accurate diagnosis and reduce unnecessary treatments for patients with suspected acute heart failure.
How similar studies have gone: Previous research has shown that combining clinical data with imaging and biomarker information can improve heart failure diagnosis, but this exact integrated rule is being tested in this setting.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult (aged ≥ 18 years) * Suspected AHF or acute dyspnea * Symptoms include shortness of breath, swelling of legs, orthopnea, paroxysmal nocturnal dyspnoea, exertional dyspnea or weight gain Exclusion Criteria: * Trauma patients * Pregnancy * Unstable patients requiring invasive airway intervention * Patients who refuse to participate
Where it's running
-
Prince of Wales Hospital
Hong Kong, Hong Kong Recruiting -
Queen Mary Hospital
Hong Kong, Hong Kong Not yet recruiting -
Tuen Mun Hospital
Hong Kong, Hong Kong Not yet recruiting
Study contacts
- Principal investigator: Kevin KC Hung, Dr. — Chinese University of Hong Kong
- Study coordinator: Theresa Hui
- Email: theresahui@cuhk.edu.hk
- Phone: +85235051698
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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.