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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03615742
Other study ID # H17-01336
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date December 1, 2018
Est. completion date December 31, 2025

Study information

Verified date March 2024
Source University of British Columbia
Contact Parteek (PJ) Johal, BCS
Phone 6048755132
Email de.study@ubc.ca
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators are studying the effects of exposure to diesel exhaust on lung inflammation in the presence and absence of an inhaled corticosteroid. Although data is mixed, studies show that asthmatics have increased lung inflammation and worse symptoms during periods of higher air pollution despite taking their anti-inflammatory corticosteroid medication. One possible reason is that air pollution exposure may decrease the ability of corticosteroids to combat inflammation. To test this volunteers will inhale either a placebo or a corticosteroid, before sitting in an exposure booth for 2 hours breathing either filtered air or diluted diesel exhaust. Samples will be collected before and after exposure to analyze the effects of budesonide and diesel exhaust exposure.


Description:

1) Purpose Inhalation of air pollutants leads to both airway inflammation, with increased cytokine expression and inflammatory cell recruitment to the airways, and to airway hyperresponsiveness, which together contribute to airway resistance and breathing difficulties. Correlational data indicate that exposure to air pollution increases inhaled corticosteroids (ICS) use in asthmatics, suggesting that steroidal anti-inflammatory medications are suboptimally effective under these conditions. However, a major issue is that no study has yet been performed specifically to determine the effects of controlled diesel exhaust (DE) exposure on responses to ICS. Furthermore, investigators need better insight into mechanisms, including the effects of epigenetic modifications and polymorphisms in oxidative stress response genes, which remain under explored. Investigators anticipate that an improved understanding of air pollution-induced ICS hyporesponsiveness (reduced effectiveness) could underpin preventative guidelines, guide ICS usage in response to environmental exposures, and inform rational pharmaceutical development. Ultimately this could lead to fewer exacerbations in asthmatic and other susceptible populations. Hypothesis: Acute exposure to DE reduces ICS-inducible gene expression in vivo in asthmatics, in part through effects on epigenetic processes. Justification: Air pollution exposure correlates with increased use of ICS inhalers in asthmatics, suggesting that ICS offer less control during periods of higher air pollution. As genes induced by ICS are critical in reducing inflammatory messenger ribonucleic acid (mRNA) and protein expression, the investigators have chosen to focus on the effects of DE on ICS-inducible gene expression as our primary endpoint. Research Method: To test this the effects of air pollution exposure on a corticosteroid, volunteers will inhale either a placebo (inhaler containing no medication) or budesonide (1.6mg), before sitting in our exposure booth for 2 hours breathing either filtered air (as a control) or diluted diesel exhaust (standardized to 300µg/m³ of particulate matter with a diameter of 2.5 micrometers or less). Volunteers will visit our lab four different times to be exposed to: 1) placebo & filtered air, 2) placebo & diesel exhaust, 3) corticosteroid and filtered air, and 4) corticosteroid and diesel exhaust. Investigators can then compare responses to each of these combinations of exposures. Investigators will take blood samples before and after volunteers complete each of these exposures to track how they affect the body. Six hours after placebo or budesonide inhalation a research bronchoscopy will be performed during which a very thin flexible tube will be inserted through the mouth and down into lungs to collect samples from each volunteer. Bronchoalveolar lavage, bronchial washes, bronchial brushes and tissue biopsies will be obtained for analysis of gene expression and epigenetic endpoints. Nasal lavage samples will also be collected to examine responses in the upper airways and blood and urine will be studied to examine systemic responses. Spirometry will be used to assess effects on airway function.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date December 31, 2025
Est. primary completion date December 31, 2025
Accepts healthy volunteers No
Gender All
Age group 19 Years to 49 Years
Eligibility Inclusion Criteria: 1. Aged 19-49 2. Have physician-diagnosed asthma confirmed by the study physician examination, spirometry, methacholine challenge provocative concentration causing a 20% fall (PC20) of <16 mg/mL, and questionnaires during a screening visit Exclusion Criteria: 1. Smoking of any kind (0.5 pack-years ever, or any current) or use of vape/vaporizing devices 2. Regular anti-histamine, NSAID, corticosteroid or other controller medication use 3. Pregnancy or breastfeeding 4. Methacholine PC20 >16 5. Relevant cardiac condition or arrhythmia 6. Body mass index of >35 7. Currently participating in another study that may interfere with this study 8. Use of either inhaled or oral corticosteroids in preceding 6 months 9. Substantial comorbidities on study physician's examination or other concerns 10. Surgery scheduled before anticipated study completion

Study Design


Intervention

Other:
Placebo
Inhalation of air through a Turbuhaler that contains no medication, as a control.
Drug:
Budesonide
1.6mg of budesonide from a Turbuhaler.
Other:
Filtered Air
Exposure to HEPA filtered air, as a control.
Diesel Exhaust
Diesel exhaust standardized to 300µg/m³ of particulate matter with a diameter of 2.5 micrometers or less (PM2.5).

Locations

Country Name City State
Canada University of British Columbia Vancouver British Columbia

Sponsors (3)

Lead Sponsor Collaborator
University of British Columbia AllerGen NCE Inc., Canadian Institutes of Health Research (CIHR)

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in DNA methylation, mRNA and protein expression attributable to diesel exhaust and inhaled corticosteroid EPIC arrays and RNA Seq will be used to determine effect of exposure(s) Baseline versus 6 hours
Secondary Modification by variants in genes governing inflammation and responses to oxidative stress after DE exposure and ICS. Genotypes will be assessed by polymerase chain reaction assay (PCR) and a gene score created for statistical interaction analysis Baseline versus 6 hours
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