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Effects of Allergen Inhalation on Adenosine Receptor Expression in Sputum and Peripheral Blood - Article


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Clinical Trial: Effects of Allergen Inhalation on Adenosine Receptor Expression in Sputum and Peripheral Blood

This study is not yet open for patient recruitment.

Sponsored by: Groniningen Institute for Asthma and COPD
Information provided by: Groniningen Institute for Asthma and COPD

Purpose

The purpose of this study is to determine whether asthmatics have different adenosine receptor expression profiles than healthy controls. We hypothesize that asthmatics will have increased adenosine receptor expression versus control subjects.

We also want to study the effects of allergen inhalation on adenosine receptor expression in asthmatics. We believe that adenosine receptor expression will be upregulated after allergen inhalation.

Both hypotheses are being tested in sputum and peripheral blood.

Condition Intervention
Asthma
Healthy
 Behavior: allergen inhalation
 Behavior: withdrawal of medication
 Procedure: sputum induction

MedlinePlus related topics:  Asthma

Study Type: Observational
Study Design: Screening, Cross-Sectional, Defined Population, Prospective Study

Official Title: Effects of Allergen Inhalation on Adenosine Receptor Expression and Mast Cell Activation in Peripheral Blood and Sputum of Asthmatics and Healthy Subjects

Further Study Details: 

Expected Total Enrollment:  20

Study start: July 2005
Last follow-up: July 2006

Eligibility

Ages Eligible for Study:  18 Years   -   50 Years,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

Asthmatic Subjects - Inclusion Criteria:

  • Clinical diagnosis of asthma
  • Steroid naive or subjects not using their inhaled steroids for the last 4 weeks, short-acting beta-agonist for rescue medication
  • FEV1 > 70% of predicted
  • Positive skin prick test for house dust mite, cat or grass pollen
  • PC20 methacholine or histamine < 8 mg/ml

Asthmatic Subjects - Exclusion Criteria:

  • Use of systemic steroids in the previous 6 weeks
  • Asthma exacerbations in the previous 6 weeks
  • Current or ex-smokers with ≥ 10 pack-years (≥ 2 pipe pack-years), ex smokers who stopped less than 1 year ago

Healthy Subjects - Inclusion Criteria:

  • No airway complaints
  • FEV1 > 90% of predicted
  • Negative skin prick test
  • PC20 methacholine or histamine > 8 mg/ml

Healthy Subjects - Exclusion Criteria:

  • Use of steroids in the previous 6 weeks
  • Current or ex-smokers with ≥ 10 pack-years (≥ 2 pipe pack-years), ex smokers who stopped less than 1 year ago

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00116311

Mieke Versluis, PhD-student      0031 50 3619171    m.versluis@path.umcg.nl

Netherlands
      University Medical Center Groningen, Department of Pulmonology, Groningen,  9713 GZ,  Netherlands
Mieke Versluis, PhD-student  0031 50 3619171    m.versluis@path.umcg.nl 
Mieke Versluis, PhD-student,  Sub-Investigator

Study chairs or principal investigators

Dirkje S Postma, prof. MD PhD,  Principal Investigator,  University Medical Center Groningen, Department of Pulmonology, hanzeplein 1, 9713 GZ Groningen, The Netherlands   

More Information

Study ID Numbers:  METc2004-253
Record last reviewed:  June 2005
Last Updated:  June 30, 2005
Record first received:  June 28, 2005
ClinicalTrials.gov Identifier:  NCT00116311
Health Authority: Netherlands: Dutch Health Care Inspectorate
ClinicalTrials.gov processed this record on 2005-07-05

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Page Updated: June 1, 2005
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