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Nebulized Budesonide for Children Who Are Hospitalized for Acute Wheezing

Phase 4
Completed
Conditions
Asthma
Acute Asthma
Interventions
Drug: % 0.9 Saline solution
Registration Number
NCT00733473
Lead Sponsor
Kecioren Education and Training Hospital
Brief Summary

The purpose of this study is to determine if adding nebulized budesonide to the systemic steroid for treatment of acute wheezing has any additive benefit in children who have hospitalized for acute wheezing.

Detailed Description

Context: Inhaled steroids reduced admission rates in patients with acute asthma, but it is unclear if there is a benefit of inhaled corticosteroids when used in addition to systemic corticosteroids. There is insufficient evidence that inhaled corticosteroids result in clinically important changes in pulmonary function or clinical scores when used in acute asthma. Similarly, it was mentioned in the Cochrane Database of Systematic Reviews that further research is needed to clarify if there is a benefit of inhaled corticosteroids when used in addition to systemic steroids.

Objective: To determine if adding nebulized budesonide to the systemic steroid for treatment of acute wheezing in hospitalized children has any benefit on, symptom score, duration of hospitalization and time to discharge from hospital.

Study Design/Setting/Participants: A double-blind, randomized, controlled trial of nebulized budesonide versus placebo for children 6 months to 6 years of age who have admitted to the hospital for acute wheezing.

Intervention: Participants will receive standard therapy including SCS, albuterol, and ipratropium bromide and will be randomly assigned to also receive either nebulized BIS or saline.

Study Measures: Differences in asthma scores, vital signs, duration of hospitalization and time to discharge from hospital will be compared between treatment groups.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Children who have recurrent wheezing attacks
  • Children who admitted to the hospital for acute wheezing
  • Clinical asthma score of 3-9
  • Parental/guardian permission (informed consent) and if appropriate, child assent
Exclusion Criteria
  • Systemic corticosteroid use in the last 30 days
  • Chronic lung diseases including cystic fibrosis
  • Immunodeficiency
  • Cardiac disease requiring surgery or medications
  • Adverse drug reaction or allergy to budesonide, albuterol, ipratropium bromide, prednisone, prednisolone, or methylprednisolone
  • Known renal or hepatic dysfunction
  • Impending respiratory failure requiring positive pressure ventilation
  • Immune deficiency
  • Gastroesophageal reflux disease
  • Suspected foreign body aspiration or croup
  • Anatomic abnormalities of the respiratory tract

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
2 Placebo saline% 0.9 Saline solutionThis arm consist 50 children with recurrent wheezing who are hospitalized for wheezing epizode. They received 2ml of nebulized saline 2 times a day upto 5 days
1 BudesonideBudesonide 0.5 mg/ml nebulesThis arm consist 50 children with recurrent wheezing who are hospitalized for wheezing epizode. They received 1 mg nebulized budesonide 2 times a day upto 5 days
Primary Outcome Measures
NameTimeMethod
Time to discharge from the hospital to home1-5 days
Secondary Outcome Measures
NameTimeMethod
Pulmonary index score1 to 5 days
Oxygen saturation1 to 5 days
Adverse reactions.1 to 5 days
Respiratory rate1 to 5 days

Trial Locations

Locations (1)

Kecioren Education and Training Hospital

🇹🇷

Ankara, Kecioren, Turkey

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