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Comparison between two different routes of Furosemide administration in Patients with Pulmonary Edema

Not Applicable
Conditions
Pulmonary edema.
Acute pulmonary edema
Registration Number
IRCT2017030332853N1
Lead Sponsor
Ahvaz Jundishapur University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
85
Inclusion Criteria

Patients with shortness of breath during the past six hours, patients with clinical signs of pulmonary edema (tachypnea, increased lung function, use of accessory muscles, crackles, wheezes and gallop rhythm), and radiographically diagnosis of pulmonary edema.
Exclusion criteria:
Cardiogenic shock and blood pressure less than 90 mmHg, noncardiogenic pulmonary edema, myocardial infarction, severe heart valve disease, history of pulmonary obstructive disease, patients requiring intubation, cardiac arrhythmias, liver failure, cancer, sensitivity to Furosemide , patient’s dissatisfaction and pregnancy.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Dyspnea severity. Timepoint: 15,30,60 and 120 minutes after treatment. Method of measurement: Dyspnea Scale criteria.
Secondary Outcome Measures
NameTimeMethod
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