CTRI/2023/07/054624
Not yet recruiting
未知
Comparative efficacy of nebulised salbutamol, salbutamol plus budesonide and salbutamol plus fluticasone in the management of acute exacerbation of bronchial asthma in children: A Randomized controlled, triple blind, three arm trial. - Nil
Dr Rachna Pasi0 sites0 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: J452- Mild intermittent asthmaHealth Condition 2: J453- Mild persistent asthmaHealth Condition 3: J454- Moderate persistent asthmaHealth Condition 4: J455- Severe persistent asthma
- Sponsor
- Dr Rachna Pasi
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Children with known asthma as defined by British Thoracic Society who will be presenting as acute exacerbation of asthma in pediatric OPD/Emergency department 2\.Children with past history of two or more episodic wheeze responsive to inhaled beta\-2 agonist and now presenting as acute exacerbation of asthma.3\.All children presenting with acute exacerbation of asthma whose parents will give written informed consent to participate in this study.
Exclusion Criteria
- •1\.Children with known asthma who will be presenting as acute exacerbation of asthma but whose parents will not give consent to participate.
- •2\.Children who will be having symptoms of acute life\-threatening asthma, chronic respiratory illness and those who took short/long acting b2 agonist or steroids within 6 hours prior to admission.
- •3\.Children who will be having symptoms or radiological evidence of acute alternate diagnosis i.e., bronchopneumonia or pleural effusion.
- •4\.Any deviation from the study treatment protocol necessitated due to clinical situation.
Outcomes
Primary Outcomes
Not specified
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