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Feasibility of Obtaining Pulse Oximetry Readings from the Oropharynx

J

Joseph D. Tobias

Status

Completed

Conditions

Surgery
Arterial Catheterization, Peripheral

Treatments

Device: Pulse oximetry

Study type

Interventional

Funder types

Other

Identifiers

NCT05690633
STUDY00003039

Details and patient eligibility

About

This is a prospective study to evaluate the feasibility of obtaining a pulse oximetry ready from the oropharynx with a standard oximeter probe that has been attached to an oral airway or a tongue blade. The study will compare the values from the peripheral pulse oximeter on a finger, toe, foot or hand with the that from the oropharyngeal oximeter. The study will also compare the saturation from an arterial blood gas (ABG) collected as standard of care with that obtained from the oropharyngeal oximeter.

Enrollment

100 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing a surgical procedure with general anesthesia and requiring an invasive arterial cannula

Exclusion criteria

  • Patients in whom an arterial cannula is not indicated for the surgical procedure
  • Patients in whom a peripheral pulse oximeter value cannot be obtained
  • Patients in whom an invasive arterial cannula cannot be placed
  • Patients with any type of intra-oral pathology or injury
  • Patients in whom access to the oropharynx is restricted or not feasible for any clinical reason

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

Oropharyngeal oximetry
Experimental group
Description:
The use of a pulse oximeter in the oropharynx on either an oral airway or a tongue blade.
Treatment:
Device: Pulse oximetry

Trial contacts and locations

1

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Central trial contact

Catherine Roth, MPH; Julie Rice-Weimer, RN

Data sourced from clinicaltrials.gov

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