COMPLETED

Oximeters and Skin Pigment: Impact of Skin Pigmentation on Accuracy of Pulse Oximetry

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Finger pulse oximetry SpO2 is widely used to estimate arterial oxygen saturation SaO2. Current Spo2 targets do not take into consideration the many variables that affect that correlation in particular skin pigmentation. This study aims to evaluate different FDA approved pulse oximeters (Nonin co-pilot, massimo Radical 7, Philips-standard of care monitor, innovo premium iP900BP, nellcor PM1000N, Nano100) with SaO2 reference values obtained by an arterial blood gas in subjects with different skin pigments measured by a skin color scale as well as self-identification of race.

Official Title

Impact of Skin Pigmentation on Accuracy of Pulse Oximetry

Quick Facts

Study Start:2023-02-27
Study Completion:2025-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05690269

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * ≥ 18 years old
  2. * Patients admitted to the Intensive Care Unit
  3. * Patient has arterial line
  1. * No signal with the oximeter
  2. * Missing digits preventing application of all probes simultaneously
  3. * No requirement for arterial blood gases
  4. * Pigmented nails, fake nails, or nail polish
  5. * Methemoglobinemia
  6. * Patient in isolation (multi-resistant bacteria, C-Difficile, COVID-19)

Contacts and Locations

Principal Investigator

Dina Gomaa, MSc
PRINCIPAL_INVESTIGATOR
University of Cincinnati

Study Locations (Sites)

University of Cincinnati
Cincinnati, Ohio, 45267
United States

Collaborators and Investigators

Sponsor: University of Cincinnati

  • Dina Gomaa, MSc, PRINCIPAL_INVESTIGATOR, University of Cincinnati

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-02-27
Study Completion Date2025-03-31

Study Record Updates

Study Start Date2023-02-27
Study Completion Date2025-03-31

Terms related to this study

Keywords Provided by Researchers

  • SpO2, SaO2,Hypoxemia

Additional Relevant MeSH Terms

  • Hypoxemia
  • Hyperoxia
  • Pigment Skin