Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01874834 · ClinicalTrials.gov registry record · NA

Cardiopulmonary Responses to Exposure to Ozone and Diesel Exhaust

A NA study, sponsored by Environmental Protection Agency (EPA).

Completed
Registry status
NA
Development phase
15
Enrollment target

NCT01874834: Completed NA study, sponsored by Environmental Protection Agency (EPA).

NCT01874834 is a NA study that has completed, run by Environmental Protection Agency (EPA). The registered enrollment target is 15 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT01874834, a NA study, has completed, sponsored by Environmental Protection Agency (EPA).

COMPLETED
Registry status
NA
Development phase
15 participants
Enrollment target

Study Summary

The US EPA Clean Air Multiyear research program is moving toward a multi-pollutant approach to the assessment of air pollution in response to recommendations by the NRC 2004 and the BOSC in 2005. Such an approach better reflects the complexity of real-world air pollution problems and parallels evolving scientific and regulatory considerations. Ozone (O3) and diesel exhaust (DE) generally are major and important components of ambient air pollution. This proposed study will address the agency's goals by investigating the cardiopulmonary health effects in healthy human subjects co-exposed to O3 and DE. The findings derived from these exposures will provide NCEA findings for risk assessments of O3 and DE, as well as the Office of Air and Radiation (includes OTAQ and OAQPS) with information relevant to possible modulation of PM-induced health effects and responses by a gaseous co-pollutant for potential standard setting. Additionally the findings will address the fundamental driving principle of the Clean Air Research strategy related to reduction of health due to air pollutant exposures.

Primary Outcome

Lung function decrements are typically expressed as changes in FEV1 and FVC. Measurements are made pre-exposure (defined as baseline, immediately post exposure, 1-4 hr post exposure, and 24 hr post exposure (follow up).

Interventions

  • OTHER ozone

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2010-08
Est. Completion 2013-01
Phase NA

What the finished NCT01874834 record still lists

NCT01874834 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 15 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which ozone is the first listed.

NCT01874834 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01874834 about?

NCT01874834 is a clinical study titled "Cardiopulmonary Responses to Exposure to Ozone and Diesel Exhaust". The US EPA Clean Air Multiyear research program is moving toward a multi-pollutant approach to the assessment of air pollution in response to recommendations by the NRC 2004 and the BOSC in 2005. Such an approach better reflects the complexity of real-world air pollution problems and parallels evolv...

What is the current status of trial NCT01874834?

This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2010-08. Estimated completion is 2013-01.

What interventions are being tested in trial NCT01874834?

The interventions under investigation include: ozone (OTHER).

Who is sponsoring clinical trial NCT01874834?

This trial is sponsored by Environmental Protection Agency (EPA), which has 9 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01874834's enrollment target sits among peer trials

15 1881st of 2000 higher than 92 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01889381 · 15 participants · Phase 2

    Human Craniomaxillofacial Allotransplantation

  • NCT02530073 · 15 participants · NA

    Trial of Fetoscopic Endoluminal Tracheal Occlusion (FETO) for CDH

  • NCT02535936 · 15 participants · NA

    Cortical Plasticity in Spastic Diplegia After Selective Dorsal Rhizotomy

  • NCT02918474 · 15 participants · NA

    Decision Making Tool in Supporting Decision Making in Contralateral Prophylactic Mastectomy in Patients With Newly Diagnosed Breast Cancer

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01874834, the US trial registry maintained by the National Library of Medicine. NCT01874834 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.