Facemasks tested for safety in endoscopy procedures
NCT ID NCT06006078
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether wearing a special facemask during upper endoscopy (a procedure to examine the stomach and esophagus) can reduce the spread of tiny particles into the air. The goal was to better understand infection risks, like COVID-19, for healthcare workers. Researchers measured particle levels in 57 patients, with half using a facemask and half without.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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57 people
The number who actually took part.
- Started
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Aug 2021
- Finished
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Oct 2021
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * All patients undergoing elective upper endoscopic procedures (upper endoscopy, ERCP, endoscopic ultrasound) with monitored anesthesia care at main campus Cleveland Clinic inpatient endoscopy unit. Exclusion Criteria: * Any patient requiring endotracheal intubation * Pregnant patients * Emergency procedures * Patients who require use of a facemask before or during the procedure due to medical necessity * Patients under the age of 18 * Non-English speaking individuals * Patients unable to provide consent. * Any procedure done outside the designated procedure room. * If in the opinion of the anesthesiologist, a subject who was randomized to the control arm requires placement of the procedural mask to augment oxygenation, the subject will be removed from the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Cleveland Clinic Foundation
Cleveland, Ohio, 44195, United States
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