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A modified clinical protocal for the diagnosis of acute dyspnea in emergecy

A modified clinical protocal for the diagnosis of acute dyspnea in emergecy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17011301
Enrollment
Unknown
Registered
2017-05-04
Start date
2017-10-01
Completion date
Unknown
Last updated
2017-05-09

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

Conditions

acute dyspnea

Interventions

LCIBX group:follow LCIBX protocal for the diagnosis of acute dyspnes
control group:follow traditional protocal for the diagnosis of acute dyspnes

Sponsors

Jiangsu Hospital of Integrated Traditional and West Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who admitted to our emergency with the chief compliant of acute dyspnea, with or without haemodynamic instability; 2. Acute dyspnea is defined as "a subjective experience of breathing discomfort that consists of qualitatively distinct sensations that vary in intensity and admitted to our emergency within 3 weeks of symptom onset"; 3. The diagnostic criteria of haemodynamic instability: (1) reasonable cause of haemodynamic instability could be fined; (2) consciousness disturbance; (3) pulse rate>100bpm or pulse couldn't be touched; (4) microcirculation collapse; (5) systolic pressure 30% of the basal value in primary hypertension patients.

Exclusion criteria

Exclusion criteria: 1. patients who can not go through pulmonary and cardiac ultrasound examination because of severe chest deformity or subcutaneous emphysema; 2. patients who abandoning treatment during hospital; 3. patients who suffering mental disorder.

Design outcomes

Primary

MeasureTime frame
heart and lung ultrasound;serum enzyme activity;ECG;chest X-ray;thoracic CT scans;

Countries

China

Contacts

Public ContactHaibin Ni

Jiangsu Hospital of Integrated Traditional and West Medicine

nhb_2002@126.com+86 13401980398

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026