Assessment and comparison of two standard protocols for management of asthma attack
Phase 3
Recruiting
- Conditions
- Acute asthma attack.Unspecified asthma with (acute) exacerbationJ45.901
- Registration Number
- IRCT20151103024853N3
- Lead Sponsor
- Ahvaz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 66
Inclusion Criteria
Patients with clinical and para clinical approved asthma with clinical presentation of acute asthma attack
Age: minimum 18 years old and maximum 65 years old
Exclusion Criteria
COPD
CHF
Pneumonia
Lung disease
Nursing mothers
Fever
Pregnancy
Administration of salbutamol in the last 6 hours
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical state. Timepoint: Before intervention, 20, 40, 60 minutes after intervention. Method of measurement: Base on alert status, talking, wizing, use of respiratory muscles.;Forced Expiratory Volum in First Secend (FEV1). Timepoint: Before intervention, 20, 40, 60 minutes after intervention. Method of measurement: Mililiter with use of Peak Flow Meter.;Peak Expiratory Flow Rate(PEFR). Timepoint: Before intervention, 20, 40, 60 minutes after intervention. Method of measurement: Mililiter with use of Peak Flow Meter.
- Secondary Outcome Measures
Name Time Method Blood pressure. Timepoint: Before intervention, 20, 40, 60 minutes after intervention. Method of measurement: mm Hg.;Pulse Rate. Timepoint: Before intervention, 20, 40, 60 minutes after intervention. Method of measurement: Rate/Minutes.;Respiratory Rate. Timepoint: Before intervention, 20, 40, 60 minutes after intervention. Method of measurement: Rate/Minutes.;Saturation of arterial blood oxygen (SO2 %). Timepoint: Before intervention, 20, 40, 60 minutes after intervention. Method of measurement: Pulse Oximetry.