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The effect of endotracheal administration of N-acetylcysteine and heparin on symptom improvement in acute respiratory distress

Phase 3
Recruiting
Conditions
lung disorder.
Respiratory disorder, unspecified
Registration Number
IRCT20190205042631N1
Lead Sponsor
Vice Chancellor of Research and Technology Shahrekord University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
26
Inclusion Criteria

Patients with acute respiratory distress syndrom and lung cantusion

Exclusion Criteria

Pregnancy
Allergy to heparin or acetylcysteine
Active bleeding

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement of respiratory symptoms. Timepoint: After seven days. Method of measurement: Checklist.
Secondary Outcome Measures
NameTimeMethod
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