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OpenTrials
Completed

NCT Number: NCT02182713

Combivent vs. Salbutamol in Patients With Metacholine Induced Bronchospasm

The purpose of this study was to evaluate whether 2 puffs of fixed combination of aerosolized 120 mcg salbutamol sulphate (equivalent to 100 mcg of the base) + 20 mcg ipratropium bromide confers significant additional protection against metacholine induced bronchoconstriction in asthmatic atopic patients when compared to 2 puffs of aerosolized 100 mcg salbutamol alone.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female patients with a diagnosis of asthma according to the American Thoracic Society Criteria
  • Patients aged 7 to 12 years inclusive
  • Patients able to perform spirometry
  • Patients with FEV1 (forced expiratory volume in the first second) ≥ 80% of predicted normal value after saline
  • Patients with PD20 (provocative dose that reduces FEV1 by 20 %) metacholine lower than 8 mg/ml
  • Patients or responsible relatives willing and able to sign an informed consent form

Exclusion criteria

  • Patients on treatment for or suspected as having glaucoma
  • Patients with known allergy of contra-indications to either salbutamol, ipratropium or their excipients
  • Patients suspected on clinical grounds to have pneumonia, pneumothorax or pneumomediastinum
  • Patients with a history of chest surgery
  • Patients with other respiratory conditions if diagnosed. These include pulmonary fibrosis, bronchiectasis, cystic fibrosis, sarcoidosis, pulmonary tuberculosis, pulmonary complications of AIDS
  • Patients requiring drugs for the treatment of the acute asthma attack other than the study drugs or oxygen
  • Patients who have been previously recruited into this study
  • Patients with myocardiopathy, pulmonary edema or other life threatening diseases, which in the judgement of the pediatrician precludes their entry into the study
  • Patients with obvious or previously diagnosed serious hepatic or renal disease
  • Patients who have been under the following drugs within the specified periods of time prior to determination of Baseline FEV1 or metacholine challenge
  • INHALED:
  • Short acting β2 agonists: 6 hours
  • Long acting β2 agonists: 12 hours
  • Ipratropium bromide: 8 hours
  • DSCG (disodium cromoglicate): 7 days
  • Nedocromil: 7 days
  • ORAL:
  • Short acting β2 agonists: 18 hours
  • Anticholinergics: 7 days
  • Short acting theophylline: 24 hours
  • Long acting theophylline: 72 hours
  • Antihistamines: 7 days
  • Astemizole: 3 months
  • Ketotifen: 3 months
  • INHALED or ORAL: Other investigational drugs: 3 months
  • INHALED or ORAL: Corticosteroids: 30 days

Treatment and study plan

Salbutamol sulfate/Ipratropium bromide

Drug

Salbutamol sulfate 120 mcg + Ipratropium bromide 20 mcg per puff

Other names: CombiventTM

Salbutamol

Drug

Salbutamol 100 mcg per puff

Other names: Ventolin®

Primary outcomes

  1. Increase in PD20 (provocative dose that reduce forced expiratory volume at one second (FEV1) by 20%)

    Time frame: Baseline and 30 minutes after treatment

Secondary outcomes

  1. Change from baseline in systolic and diastolic blood pressure

    Time frame: Baseline, 30 and 60 min after treatment

  2. Change from baseline in heart rate

    Time frame: Baseline, 30 and 60 min after treatment

  3. Change from baseline in respiratory rate

    Time frame: Baseline, 30 and 60 min after treatment

  4. Occurrence of adverse events

    Time frame: up to 8 days

  5. SaO2 (oxygen saturation) during metacholine challenge

    Time frame: continuously after adminstration of study drug

Sponsors and collaborators

Lead sponsor

Boehringer Ingelheim

Industry

Registry information

Important dates

Study start
1998
Primary completion
1998
First posted
Jul 8, 2014
Registry last updated
Jul 8, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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