Asthma Management Project University Leiden

Sponsor
Leiden University Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT00279188
Collaborator
The Netherlands Asthma Foundation (Other)
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Study Details

Study Description

Brief Summary

The long-term course of asthma shows variable outcome with regard to the incidence of exacerbations and the decline of lung function over time. The present study aimed:

  1. to investigate whether asthma management additionally guided by the degree of bronchial hyperresponsiveness leads to a better outcome

  2. to examine the predictors among clinical and inflammatory disease markers of the long-term decline in lung function

Condition or Disease Intervention/Treatment Phase
  • Procedure: Guiding therapy by bronchial hyperrsponsiveness
N/A

Detailed Description

Asthma is associated with a specific inflamma¬tory state of the airways. Assuming that the degree of airway inflammation is a determinant for the long-term disease outcome, it follows that, asthma therapy should be aimed at maximal reduction of airway inflammation, in addition to reducing symptoms. However, according to current guidelines, therapy should only be directed to the clinical severity of the disease. There is increasing evidence that bronchial hyper¬respon¬siveness can be used as a non-invasive reflection of airway inflamma¬tion [29]. However, it is still unknown whether bronchial responsiveness provides relevant additional information for adjusting therapy during follow-up of patients with asthma. Therefore, in this study we will:

  1. compare the disease outcome in two parallel groups of patients with asthma, receiving therapy aimed at either clinical severity only, or therapy aimed at both clinical severity, and bronchial hyper¬responsiveness to methacho¬li¬ne. The outcome will be assessed at three levels. First, the severity, second, lung function and bronchial responsive¬ness, and third, humoral, cellular, and histological indices of airway inflamma¬tion. To that end we will assess symptoms, lung function, bronchial respon¬siveness, and immunological parameters in blood, every three months. Furthermore, a bronchos¬copy with a bronchoalveolar lavage and bronchial biopsy will be carried out to provide for material for immunologic and pathologic anatomical examination, at the beginning and at the end of the study.

  2. analyse the predictors among clinical- and inflammatory parameters of exacerbations and long-term decline in lung function during long-term follow-up

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single
Primary Purpose:
Treatment
Official Title:
Asthma Management Project University Leiden
Study Start Date :
May 1, 1992
Study Completion Date :
Sep 1, 2008

Outcome Measures

Primary Outcome Measures

  1. Exacerbations []

  2. Post-bronchodilator FEV1 []

Secondary Outcome Measures

  1. Bronchial hyperrsponsiveness []

  2. Airway inflammationn in bronchial biopsies []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
Exclusion Criteria:
  • oral steroids

Contacts and Locations

Locations

Site City State Country Postal Code
1 Leiden University Medical Center Leiden Netherlands NL-2300 RC

Sponsors and Collaborators

  • Leiden University Medical Center
  • The Netherlands Asthma Foundation

Investigators

  • Study Chair: Peter J. Sterk, MD, PhD, Leiden University Medical Center

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00279188
Other Study ID Numbers:
  • AF 3.2.92.45, AMPUL
  • AF 3.2.92.45
First Posted:
Jan 19, 2006
Last Update Posted:
Jan 19, 2006
Last Verified:
Sep 1, 2004

Study Results

No Results Posted as of Jan 19, 2006