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Study to Assess the Efficacy of Ipratropium Bromide Associated With High Dose Salbutamol by Repeated Nebulisation Versus Repeat Nebulisation of Salbutamol Alone, in Acute Asthmatic Attacks in Young Children

Phase 4
Terminated
Conditions
Asthma
Interventions
Registration Number
NCT02235428
Lead Sponsor
Boehringer Ingelheim
Brief Summary

To determine whether addition of ipratropium bromide to salbutamol nebulisations produces significantly greater bronchodilation in young children presenting to an emergency department with an acute attack of asthma

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
3
Inclusion Criteria
  • Boys or girls between 3 and 6 years old
  • Presenting to emergency departments with an acute asthmatic attack
  • Requiring nebulised bronchodilator therapy
  • Rint increased by 200 % compared to theoretical Rint
  • Signed, informed consent obtained from the child's parents/legal guardian in accordance with current national legislation and good clinical practice (GCP) defined by the International Conference on Harmonization (ICH)
Exclusion Criteria
  • Ipratropium bromide received within four hours before admission
  • First acute asthmatic attack
  • Hospital admission to intensive care with asthma within six months before inclusion
  • Hospital admission for asthma during the month prior to inclusion
  • Corticosteroid-dependent asthma (oral corticosteroid therapy) or recently stopped corticosteroid therapy
  • Concomitant cardiac disease
  • Life threatening disease requiring immediate management; including: silent chest on auscultation, cyanosis, bradycardia less than 60 beats/min (bpm), confusion, coma
  • Hypersensitivity to ipratropium bromide, salbutamol, or to any of their excipients
  • Renal or hepatic insufficiency
  • Poorly controlled diabetes
  • Patients suffering from a disease considered to be severe by the investigator and which, in the opinion of the investigator, could interfere or invalidate the measurements performed in the trial
  • Past history of lung surgery
  • Major respiratory disease: pulmonary fibrosis, bronchiectasis, sarcoidosis, tuberculosis, respiratory disease due to AIDS, cystic fibrosis
  • Patients unable to follow with protocol or correctly undergo the evaluations
  • Patients who are taking part in another clinical trial during this trial or who have done so within the month before the trial
  • Previous participation in this trial

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
SalbutamolPlacebo-
Ipratropium bromideIpratropium bromide-
Ipratropium bromideSalbutamol-
SalbutamolSalbutamol-
Primary Outcome Measures
NameTimeMethod
Changes from baseline in pulmonary resistance (Rint) between T0 and T120Baseline, 120 minutes after drug administration
Secondary Outcome Measures
NameTimeMethod
Assessment of wheezing on a 4-point scaleUp to 120 minutes after drug administration
Changes in respiratory rateUp to 120 minutes after drug administration
Changes in measurement of pulmonary resistanceUp to 120 minutes after drug administration
Number of patients with adverse eventsUp to 17 days after last drug administration
Assessment of accessory muscle recruitment on a 4-point scaleUp to 120 minutes after drug administration
Hospital Admission rate120 minutes after drug administration
Assessment of dyspnoea on a 4-point scaleUp to 120 minutes after drug administration
Changes in Oxygen Saturation (ambient air)Up to 120 minutes after drug administration
Number of patients dropped out because of lack of efficacyUp to 120 minutes after drug administration
Number of patients with clinical significant findings in blood pressureUp to 120 minutes after drug administration
Number of patients dropped out because of adverse eventsUp to 17 days after last drug administration
Number of patients with clinical significant findings in heart rateUp to 120 minutes after drug administration
Assessment of Patient Status by investigator on a 3-question list72 hours after drug admimistration
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