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Emission Patterns of Respiratory Pathogens

Emission Patterns of Respiratory Pathogens

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03491020
Enrollment
0
Registered
2018-04-06
Start date
2024-12-31
Completion date
2025-05-31
Last updated
2025-01-15

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

Conditions

Pathogen Transmission

Keywords

Emission Patterns, Respiratory, Aerosolization, Airborne

Brief summary

Airborne transmission represents one of the most rapidly spreading and dangerous dissemination mechanisms for pathogens. Public health strategies to prevent and control the often explosive outbreaks associated with such pathogens are: 1) vaccination and treatment, if available, 2) isolation and barrier precautions such as face masks, and 3) decontamination of the exposed areas and surfaces. A lack of understanding how these pathogens are transmitted hampers the ability to develop effective prevention measures. This study will be used to collect preliminary data of the emission patterns of respiratory pathogens.

Detailed description

Airborne transmission represents one of the most rapidly spreading and dangerous dissemination mechanisms for pathogens. The study team have been investigating bacterial and viral transmission routes and barrier precautions. In a recent clinical study, it was observed that Measles virus RNA was detected from a patient for at least up to 10 feet. In addition, the group has been studying barrier precautions (facemasks) for their ability to prevent the spread of aerosolized viruses. Finally, in a controlled lab setting the investigators have assessed the impact of environmental conditions (temperature, humidity) on pathogen transmission and the effect of UV-C light to prevent the spread of influenza. The purpose of this observational study is to describe the human aerosolization patterns of respiratory pathogens. The study team hypothesizes that the emission patterns of specific airborne pathogens varies between individual patients.

Interventions

None listed

Sponsors

Wake Forest University Health Sciences
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients \>18 years of age admitted to the ED or an inpatient care unit of Wake Forest Baptist Medical Center (WFBMC) * Positive

Exclusion criteria

* positive respiratory pathogen tests

Design outcomes

Primary

MeasureTime frameDescription
particle size distribution patterns: ICUthroughout study completion, up to 7 daysThis outcome measure will determine the particle size distribution patterns of the pathogen in the intensive care unit (ICU).
particle size distribution patterns: non-ICU settingthroughout study completion, up to 7 daysThis outcome measure will determine the particle size distribution patterns of the pathogen in the non-intensive care unit (ICU).
quantities of the pathogen: ICUthroughout study completion, up to 7 daysThis outcome measure will determine the quantities of the pathogen in the intensive care unit (ICU).
quantities of the pathogen: non-ICU settingthroughout study completion, up to 7 daysThis outcome measure will determine the quantities of the pathogen in the non-intensive care unit (ICU).
spatial model: ICUthroughout study completion, up to 7 daysThis outcome measure will establish a spatial model (1 foot vs. 3- feet vs. 8-10 feet) of airborne pathogen dispersal in the ICU.
spatial model: non-ICU settingthroughout study completion, up to 7 daysThis outcome measure will establish a spatial model (1 foot vs. 3- feet vs. 8-10 feet) of airborne pathogen dispersal in a non-ICU setting.
correlation between the human aerosolization patterns and the severity of illnessthroughout study completion, up to 7 daysThis outcome measure is to determine the correlation between the human aerosolization patterns and the severity of illness (fever, respiratory symptoms, malaise) in individual participants.

Outcome results

None listed

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