Extra-fine Formoterol/Beclomethasone in Asthmatic Crisis
Asthma, Asthmatic Crisis
About this trial
This is an interventional treatment trial for Asthma focused on measuring formoterol/beclomethasone in asthmatic crisis, asthmatic crisis treatment
Eligibility Criteria
Inclusion Criteria:
- previous asthma diagnosis by physician
- spirometry with quality grade A, B or C
- presenting with asthmatic crisis in emergency room
Exclusion Criteria:
- imminent respiratory arrest
- respiratory comorbidities (COPD, cystic fibrosis, interstitial lung disease, pneumothorax, bronchiectasis)
- use of systemic steroids in 3 months previous
- allergy to steroids
- Peripheral capillary oxygen saturation (SpO2) less than 88%.
Sites / Locations
- National Institute of Respiratory Diseases
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
Extra fine Formoterol/Beclomethasone
Placebo
Group receiving the drug additional to standard treatment standard treatment consisting in: Albuterol 2.5 mg via nebulizer at baseline, 0, 20, 40 minutes + Systemic steroid (methylprednisolone 60 mg) at the moment of evaluation + formoterol/beclomethasone, 3 puffs administered via aerochamber at baseline (0), 20, 40 minutes
Group receiving placebo additional to standard treatment consisting in: Albuterol 2.5 mg via nebulizer at baseline (0), 20, 40 minutes + Systemic steroid (methylprednisolone 60 mg) at the moment of evaluation + Placebo, 3 puffs administered via aerochamber at baseline (0), 20, 40 minutes