Status:

COMPLETED

Health Effects of Diesel Exhaust in Asthmatic Patients: A Real-world Study in a London Street

Lead Sponsor:

Imperial College London

Collaborating Sponsors:

Health Effects Institute

Conditions:

Asthma

Eligibility:

All Genders

18-55 years

Phase:

NA

Brief Summary

Acute exposure to diesel exhaust under normal city conditions leads to a worsening of symptoms of asthma, with reduction in lung function in asthmatic nonsmoking adults, dependent on the exposure dose...

Detailed Description

The investigators will recruit 60 nonsmoking asthmatics of mild and of moderate severity. They will be exposed to Oxford St. or to Hyde Park for 2 hours each, at a walking pace. Real time exposure to ...

Eligibility Criteria

Inclusion

  • Inclusion Criteria:
  • Subjects will be selected according to the current severity of their asthma; thirty from Steps 1 and 2 and thirty from Step 3 of the World Health Organization (WHO) Global Initiative for Asthma (GINA) asthma guidelines. These will include mild and moderate asthmatic states. Depending on baseline FEV1, subjects will undergo either a methacholine bronchial hyperresponsiveness assessment or airways reversibility testing. Subjects with normal FEV1 (\>80% predicted) or normal FEV1/FVC ratio will undergo methacholine challenge. Subjects with FEV1 \<80% predicted will undergo airways reversibility testing. Subjects must have either a PC20 of less than 8mg/ml methacholine, or improvement in FEV1 of 12% or more, following inhalation of short acting β-agonist (salbutamol 200μg from metered dose inhaler \[MDI\]). Skin prick testing will be conducted for common allergens (house dust mite, grass pollen, aspergillus fumigatus and cat hair). The results will only be for descriptive purposes, not as subject inclusion/exclusion criteria. Subjects may be atopic or non-atopic (according to history and allergy testing).

Exclusion

    Key Trial Info

    Start Date :

    May 1 2003

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    August 1 2006

    Estimated Enrollment :

    60 Patients enrolled

    Trial Details

    Trial ID

    NCT00127062

    Start Date

    May 1 2003

    End Date

    August 1 2006

    Last Update

    November 5 2019

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