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Clinical Trials/NCT05680831
NCT05680831
Recruiting
Phase 1

Pulmonary and Inflammatory Responses Following Exposure to a Low Concentration of Ozone or Clean Air for 6.6 Hours With Moderate Exercise in Healthy Young Adults

Martin W. Case1 site in 1 country60 target enrollmentOctober 13, 2022

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Lung Injury, Acute
Sponsor
Martin W. Case
Enrollment
60
Locations
1
Primary Endpoint
FVC
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

Purpose: The primary purpose of this study is to measure pulmonary function, symptoms, and pulmonary inflammatory responses in healthy young adults during and immediately after exposure to a low concentration of ozone (0.070 ppm) or clean air for 6.6 hours while undergoing moderate intermittent exercise. This concentration is the current EPA NAAQS standard for ozone.

Detailed Description

Potential health effects of ozone have been extensively studied over decades at various levels of exposure concentration and for varying time periods in young healthy adult subjects. Effects of ozone have been well documented particularly for decrements of lung function and an influx of neutrophils and other markers of pulmonary inflammation. The majority of those studies were done at ozone concentrations between 0.12 and 0.40 ppm, considerably higher than the current EPA NAAQS ozone standard of 0.070 ppm, and at exposure durations of two hours, even though the current standard is an 8-hour standard. However, a small number of studies have assessed changes in lung function following exposure to low levels of ozone for several hours. These latter studies have shown that exposure to ozone for 6.6 hours at concentrations between 0.06 and 0.08 ppm causes mild reversible decrements in lung function (1.7-10%) as measured by forced vital capacity (FVC) and forced expired volume at 1 s (FEV1) immediately after exposure in healthy young adults. In addition, in one study an increase in ozone-induced neutrophils was seen in induced sputum following exposure to 0.06 ppm ozone (8) and in bronchoalveolar lavage fluid) following exposure to 0.08 ppm ozone (9). The EPA is considering whether the current ozone NAAQS standard at 0.070 is protective and has asked EPA researchers to conduct a study similar to those done at 0.06 and 0.08 ppm.

Registry
clinicaltrials.gov
Start Date
October 13, 2022
End Date
February 1, 2025
Last Updated
3 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Martin W. Case
Responsible Party
Sponsor Investigator
Principal Investigator

Martin W. Case

Clinical Studies Coordinator

Environmental Protection Agency (EPA)

Eligibility Criteria

Inclusion Criteria

  • Healthy men and women between 18 and 35 years of age.
  • Physical conditions allowing sustained moderate exercise for 6.6 hours.
  • Normal lung function (NHANES III):
  • FVC \> 80 % of that predicted for gender, ethnicity, age and height.
  • FEV1 \> 80 % of that predicted for gender, ethnicity, age and height.
  • FEV1/FVC ratio \> 80 % of predicted values
  • Oxygen saturation \> 94 %.
  • Total symptom Score no greater than 20 (out of a possible 60-see accompanying score sheet) with a value no greater than 3 for any one score. No more than one score may be equal to 3.

Exclusion Criteria

  • Individuals with a diagnosis of COVID-19 and/or hospitalized for COVID-
  • Individuals who are not "up to date," \[meaning a person has received all recommended COVID-19 vaccines, including any booster dose(s) when eligible with their COVID vaccines as defined by the CDC.\]
  • A history of acute and chronic cardiovascular disease, chronic respiratory disease, diabetes,rheumatologic diseases, immunodeficiency state.
  • An acute respiratory illness within 4 weeks.
  • Subjects who are asthmatic or have a history of asthma.
  • Allergic to chemical vapors or gases.
  • Any allergic symptoms during the time of participation in the study
  • Female subjects who are currently pregnant, attempting to become pregnant or breastfeeding
  • Subjects currently taking mega doses of vitamins and supplements, homeopathic/naturopathic medicines or medications which may impact the results of the ozone challenge or interfere with any other medications potentially used in the study (to include systemic steroids and beta blockers). Medications not specifically mentioned here may be reviewed by the investigators prior to a subject's inclusion in the study.
  • Current and past smokers within 2 years, or subjects with a smoking history of at least a pack of cigarettes a day for more than 10 years over your lifetime. This includes vaping, hookah,and e-cigarettes.

Outcomes

Primary Outcomes

FVC

Time Frame: measured (pre) before starting 6.6 hours of exercise

forced vital capacity

Change in FVC

Time Frame: change measured (post) immediately after 6.6 hours of exercise

change in forced vital capacity

Change in FEV1

Time Frame: change measured (post) immediately after 6.6 hours of exercise

change in forced expiratory volume in 1 second

FEV1

Time Frame: measured (pre) before starting 6.6 hours of exercise

forced expiratory volume in 1 second

Secondary Outcomes

  • % neutrophils collected by induced sputum(baseline: training/qualification day)
  • change in % neutrophils collected by induced sputum(18 hours post exposure)

Study Sites (1)

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