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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05454930
Other study ID # STUDY00001196
Secondary ID K24ES013195RD-83
Status Completed
Phase N/A
First received
Last updated
Start date January 2015
Est. completion date December 2016

Study information

Verified date July 2022
Source University of Washington
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators will assess the vascular effects of riding in a car in heavily trafficked roadways, and whether filtering the car's air reduces those effects.


Description:

In this double-blind, crossover trial, randomized to order, recruited participants will be screened and then will accompany the study team on three typical commutes on separate days with sufficient washout (i.e., three weeks) between drives. One day this will occur with an effective filter system in the vehicle and the other two days without effective filtration; ineffective filtration is the most typical actual vehicle condition. Subjects will be unaware of the filtration conditions of the commute on that day. Each subject's experimental sessions will occur at the same time of day and will be separated by at least 21 days. The two sessions (either filtered air or traffic-derived entrained air) will be 120 minutes in duration and will encompass routes on heavily traveled roadways in the Seattle area. Before subjects begin the commute trials, they will go through the consent process and a series of screening tests. The study investigators will assess a series of measures regarding vascular function before and after each drive.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date December 2016
Est. primary completion date July 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 49 Years
Eligibility Inclusion Criteria: - healthy Exclusion Criteria: - asthma, - high blood pressure, - diabetes, - high cholesterol, - other chronic conditions requiring ongoing medical care.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Filtered Air
The vehicle is fitted with a (High-Efficiency Particulate Absorbing, HEPA) filter device incorporating a charcoal filter, as well as an augmented cabin filter

Locations

Country Name City State
United States University of Washington Medical Center Seattle Washington

Sponsors (3)

Lead Sponsor Collaborator
University of Washington Environmental Protection Agency (EPA), National Institute of Environmental Health Sciences (NIEHS)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Brachial Artery Diameter from Pre-Drive to Post-Drive Ultrasound assessment of brachial artery diameter, in millimeters. 30 minutes before 120 minute driving session; 30 minutes post driving session
Primary Change in Blood Pressure from Pre-Drive to During-Drive and Post-drive systolic and diastolic blood pressure measured in mmHg 10 minutes before driving session; 15, 30, 45, 60, 75, 90, 100, 120 minutes following start of (120 minute) driving session; 10 minutes, 1.5 hours, 3.5 hours, 6 hours, 24 hours after end of driving session.
Primary Change in Retinal Arteriolar Diameter from Pre-Drive to Post-Drive measured by retinal photography, image analysis, in micrometers 30 minutes before 120 minute driving session; 30 minutes post driving session
Primary Gene Expression and DNA methylation analysis in circulating mononuclear cells; determined via fold change in abundance 30 minutes before 120 minute driving session; 30 minutes, 5 hour, and 24 hours post-driving session
Secondary circulating stress hormone cortisol by chemiluminescence (ng/mL) 30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving session
Secondary complete blood count with differential laboratory values for hematologic indices (cells/uL) 30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving session
Secondary inflammatory marker interleukin-6 interleukin-6 determined by chemiluminescence (pg/mL) 30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving session
Secondary inflammatory marker c-reactive protein C-reactive protein by immunoturbidimetry (ug/mL) 30 minutes before 120 minute driving session; 5 hour and 24 hours post-driving session
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