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The Effect of a Retrofit Particle Trap on the Vascular Effects of Diesel Exhaust Inhalation

The Effect of a Retrofit Particle Trap on the Vascular Effects of Diesel Exhaust Inhalation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00745446
Enrollment
18
Registered
2008-09-03
Start date
2007-09-30
Completion date
2008-02-29
Last updated
2008-09-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Disease

Keywords

Air pollution, Diesel exhaust, Endothelial function, Vascular function, Particle trap, Thrombosis, effects, inhalation

Brief summary

The purpose of this study is to determine whether a retrofit particle trap can reduce the adverse vascular responses to diesel exhaust inhalation

Detailed description

18 subjects healthy male volunteers will be recruited at Umeå University. In a randomised, double blind 3 way crossover trial, subjects will be exposed to filtered air, diesel exhaust (300mcg/m3) or filtered diesel exhaust for 1 hour during intermittent exercise. 2 hours following the exposure, thrombogenicity will be assessed using the Badimon chamber - an ex-vivo model of thrombosis formed under constant flow conditions. Forearm blood flow in response to infused intra-brachial vasodilators will be measured using venous occlusion plethysmography 6 hours after the exposure. Arterial stiffness will be measured using peripheral arterial applanation tonometry in the hour post-exposure. Blood samples will be collected at timepoints over the 24 hours after exposure.

Interventions

Forearm venous occlusion plethysmography with intra-arterial infusion of Acetylcholine (5-20mcg/min), bradykinin (30-300mcg/min), sodium nitroprusside (2-8mcg/min) and Verapamil (2-10 mcg/min) into non-dominant brachial artery

Sponsors

Umeå University
CollaboratorOTHER
University of Edinburgh
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy male volunteers

Exclusion criteria

* Intercurrent illness * Smoking * Significant occupational exposure to air pollution * Regular medication usage

Design outcomes

Primary

MeasureTime frame
Forearm blood flow in response to infused intra-arterial vasodilators6 hours post-exposure

Secondary

MeasureTime frame
Arterial stiffness measured by applanation tonometryIn the 1 hour following exposure
Thrombogenicity measured using the Badimon chamber - an ex-vivo model of thrombosis under conditions of continuous flow2 hours after the exposure
Exhaled nitric oxide - a marker of pulmonary inflammation1 hour & 6 hours after exposure
Endogenous fibrinolytic capacity - measured as net release of t-PA in response to infused bradykinin6 hours after exposure
Biochemical markers of systemic inflammationBaseline, 2, 6 & 24 hours

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026