comparison of effects of nebulised Frusemide and placebi in patients with acute dyspnea transmited by EMS
Phase 3
Recruiting
- Conditions
- acute dyspnea.Dyspnea
- Registration Number
- IRCT20171014036753N2
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
all patient between 18 to 75 years old with dyspnea who transmitted to hospitals by EMS
Exclusion Criteria
not willing to participate in the study
history of susceptibility to sulfa drugs
unstable hemodynamics; requiring mechanical ventilation; decreased consciousness, accompany with another illness requiring treatment in the first 10 minutes of treatment with digoxin, beta blocker, beta-agonist and calcium; need to have another inhaling treatment in the first 10 minutes and need to have non-invasive ventilation.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method