Pediatric Source Control for Hazardous Particulate Exposure in Aerosol Generating Procedures

Withdrawn before enrolling · Not applicable

Conditions studied: Risk Reduction

In brief

There are two purposes of this study. The first purpose is to determine the exposure seen by medical providers (e.g. anesthesiologists, surgeons, and nurses) to infectious and smoke particulates generated during anesthesia-related aerosol generating medical procedures (AGMPs) and pediatric otolaryngologic surgeries (with and without an intubated airway). The second goal of this study is to apply a local exhaust ventilation system (LEVS) to re-evaluate the exposure seen by the same medical providers during the same AGMPs and surgeries.

Key facts

Study ID

NCT04577209

Run by

Stanford University

People needed

0

Starts

2025-05-01

Expected to finish

2026-05-01

Last updated by the study team

2025-05-04

Who can join

Age: 2 and older, up to 18. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• children receiving anesthesia-related aerosol generating medical procedures

You may not qualify if…

• patients with positive COVID symptoms
• positive preoperative COVID testing

Where it is running

• Lucile Packard Childrens Hospital — Stanford, California, United States

Full record on ClinicalTrials.gov

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