A Comparison of Combivent UDV (Ipratropium 500mcg and Salbutamol 2.5mg) and Salbutamol UDV Alone (2.5mg)

Launched by BOEHRINGER INGELHEIM · Jan 9, 2006

Keywords

ClinConnect Summary

A Comparison of Ipratropium 500mcg and salbutamol 2.5mg (Combivent UDV) and salbutamol UDV alone (2.5mg) in a Double-blind, Efficacy and Safety Study in Asthmatic Children with Severe Acute Exacerbation

Study Hypothesis:

Several studies, including a study conducted in an emergency room setting, demonstrated that the addition of ipratropium bromide, an anticholinergic drug, to standard salbutamol therapy significantly improves pulmonary function as compared to salbutamol alone.

Comparison(s):

Ipratropium bromide 500 mcg plus salbutamol 2.5mg (Combivent) vs salbutamol (2.5mg) alone given ...

Gender

ALL

Eligibility criteria

• • INCLUSION CRITERIA
• • 1. All patients must have a known history of asthma and present to the hospital/clinic with severe acute exacerbation.
• • 2. Male or female patients 2 to 10 years of age.
• • 3. Parents or legal guardians of patients must sign an Informed Consent Form prior to participation in the trial.
• • EXCLUSION CRITERIA
• • 1. Patients with known or suspected hypersensitivity to study drugs
• • 2. Patients with medical condition that would contraindicate the use of beta2-adrenergic or anticholinergic medications
• • 3. Patients with first wheezing episode only
• • 4. Prior intubation for asthma for more than 24 hours
• • 5. Patients who used ipratropium within six hours prior to consultation
• • 6. Patients with concurrent stridor or possible presence of intra-thoracic foreign body
• • 7. Patients with disease known to have chronic effect on respiratory function ( e.g., cystic fibrosis or cardiac disease)
• • 8. Patients requiring immediate resuscitation or airway intervention
• • 9. With psychiatric disease or psychosocial problems
• • 10. Patients on other investigational drugs or have used any other investigational drugs within the past month