Pulmonary and Inflammatory Responses Following Exposure to a Low Concentration of Ozone or Clean Air

Symptoms and Signs Clinical Trial

— LOCONOZ2  

Official title:

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05680831
• Other study ID #: IRB# 21-3193
• Status: Recruiting
• Phase: Phase 1
• Start date: October 13, 2022
• Est. completion date: February 1, 2025

Study information

• Verified date: January 2023
• Source: Environmental Protection Agency (EPA)
• Contact: Martin W Case, B.S.
• Phone: 919-966-6211
• Email: case.martin[@]epa.gov
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: February 1, 2025
• Est. primary completion date: February 1, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 35 Years

Eligibility

Inclusion Criteria:

1. Healthy men and women between 18 and 35 years of age.

2. Physical conditions allowing sustained moderate exercise for 6.6 hours.

3. Normal lung function (NHANES III):

1. FVC > 80 % of that predicted for gender, ethnicity, age and height.

2. FEV1 > 80 % of that predicted for gender, ethnicity, age and height.

3. FEV1/FVC ratio > 80 % of predicted values

4. Oxygen saturation > 94 %.

5. 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:

1. Individuals with a diagnosis of COVID-19 and/or hospitalized for COVID-19.

2. 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.]

3. A history of acute and chronic cardiovascular disease, chronic respiratory disease, diabetes,rheumatologic diseases, immunodeficiency state.

4. An acute respiratory illness within 4 weeks.

5. Subjects who are asthmatic or have a history of asthma.

6. Allergic to chemical vapors or gases.

7. Any allergic symptoms during the time of participation in the study

8. Female subjects who are currently pregnant, attempting to become pregnant or breastfeeding

9. 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.

10. 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.

11. Uncontrolled hypertension (> 140 systolic, > 90 diastolic). Blood pressure readings equal to or greater that 140 Systolic and equal to or greater that 90 diastolic.

12. Subjects who do not understand or speak English

13. Unspecified illnesses, which in the judgment of the investigator might increase the risk associated with ozone inhalation challenge or exercise, will be a basis for exclusion.

Temporary exclusion criteria:

1. Individuals who have had an acute respiratory illness within 4 weeks.

2. Individuals who have active allergies.

3. Individuals that have engaged in strenuous exercise within 24 hours of any study visit.

4. Individuals unable to avoid drinking alcohol for 24 hours prior to all study visits.

5. Individuals who have been exposed to smoke and fumes for 24 hours before all visits.

6. Individuals that have used an ozone-based home air purifier for 24 hours before all visits.

7. Individuals that have eaten or drank anything for 2 hours prior to the sputum training/screening day visit.

8. Individuals should avoid caffeine for 12 hours prior to all study visits.

9. Individuals should refrain from all over the counter anti-inflammatory agents including those for allergies, and anti-inflammatory drugs or antioxidants for a period of one week prior to the train and to the exposure.

10. Individuals that have been exposed to or have consumed any agent or have undertaken any activity within 24 hours of any study visit that the investigators believe may compromise the results of the study. -

Related Conditions & MeSH terms

• Acute Lung Injury
• Lung Injury
• Lung Injury, Acute
• Symptoms and Signs

Intervention

Biological:
• 0.070 ppm ozone concentration
The concentration of ozone a subject will randomly receive on a visit for 6.6 hours in a controlled atmospheric chamber while performing moderate intermittent exercise.
• Clean air (0.0 ppm ozone)
Same subject will randomly receive clean air on another visit separated by at least one week for 6.6 hours in the same controlled atmospheric chamber while performing moderate intermittent exercise.

Locations

Country	Name	City	State
United States	EPA Human Studies Facility	Chapel Hill	North Carolina

Sponsors (2)

Lead Sponsor	Collaborator
Martin W. Case	University of North Carolina

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	FVC	forced vital capacity	measured (pre) before starting 6.6 hours of exercise
Primary	Change in FVC	change in forced vital capacity	change measured (post) immediately after 6.6 hours of exercise
Primary	FEV1	forced expiratory volume in 1 second	measured (pre) before starting 6.6 hours of exercise
Primary	Change in FEV1	change in forced expiratory volume in 1 second	change measured (post) immediately after 6.6 hours of exercise
Secondary	% neutrophils collected by induced sputum	Subjects will breathe a hypertonic saline solution from an ultrasonic nebulizer through a mouthpiece at saline concentrations of 3%, 4%, and 5%. After each inhalation period subjects be asked to cough up the expectorate in a sterile cup for analysis of neutrophil cells influx	baseline: training/qualification day
Secondary	change in % neutrophils collected by induced sputum	Subjects will breathe a hypertonic saline solution from an ultrasonic nebulizer through a mouthpiece at saline concentrations of 3%, 4%, and 5%. After each inhalation period subjects be asked to cough up the expectorate in a sterile cup for analysis/quantitation of neutrophil cells influx	18 hours post exposure