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Diesel Exhaust Particles and Leukotriene Production

Withdrawn
Conditions
Allergic Rhinitis
Registration Number
NCT00915447
Lead Sponsor
University of California, Los Angeles
Brief Summary

The purpose of this study is to measure the effects of allergens and/or diesel exhaust particles in the nose to learn more about allergic responses in individuals with cat allergic rhinitis.

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  1. Age 18 to 65 years old.
  2. Positive prick (epicutaneous) skin test to standardized cat with a wheal equal to or greater than 3 mm and with a surrounding flare.
  3. Ability to give informed consent.
Exclusion Criteria
  1. Pregnancy or breast-feeding. (Pregnancy and the period during breast feeding can affect nasal congestion and be a confounder in this regard.)
  2. Systemic corticosteroid use within the previous three months or anytime during the challenge protocol.
  3. Topical nasal corticosteroid use within the past month or anytime during the challenge protocol.
  4. Systemic antihistamines or decongestant use within past two weeks or anytime during the trial.
  5. Chronic sinusitis or chronic non-allergic rhinitis.
  6. Use of reserpine.
  7. Cigarette smoking within the past year or during the challenge protocol
  8. Use of topical nasal antihistamines, chromoglycolates (chromolyn, Cromlon®), decongestants or non-steroidal anti-inflammatory agents (NSIADS) within the preceding week or anytime during the challenge protocol.
  9. Present or treatment within the past 10 years with allergy immunotherapy (injections).
  10. Present or past treatment with anti-IgE therapy.
  11. Any unusual exposure to air pollutants (e.g., working as a diesel mechanic) that, in the opinion of the investigators, might compromise the individual's ability to participate in the study.
  12. Living arrangement where the subject has a cat dwelling within the subject's habitation.
  13. Any serious heart, lung, neurological or kidney disease that in the opinion of the investigators would impair the individual's ability to participate in the study.
  14. Use of asthma-required medications.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of California, Los Angeles

🇺🇸

Los Angeles, California, United States

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