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Trial record 22 of 619 for:    oximeter

Pulse Oximeter Test

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT03569163
Recruitment Status : Completed
First Posted : June 26, 2018
Last Update Posted : June 26, 2018
University of California, San Francisco
Information provided by (Responsible Party):
Spry Health

Brief Summary:
Assessment of Spry Health's Loop oximetry accuracy in profound hypoxia

Condition or disease Intervention/treatment
Hypoxia Device: Spry Loop oximeter

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Study Type : Observational
Actual Enrollment : 11 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Accuracy of Pulse Oximeters With Profound Hypoxia
Actual Study Start Date : September 1, 2017
Actual Primary Completion Date : October 30, 2017
Actual Study Completion Date : October 30, 2017

Intervention Details:
  • Device: Spry Loop oximeter
    Oximetry was performed on the subjects and accuracy was determined based on comparison with blood gas analysis.

Primary Outcome Measures :
  1. Oximetry Accuracy [ Time Frame: 30 minutes ]
    RMSE of pulse oximeter

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 50 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
11 healthy adults

Inclusion Criteria:

  • Good general health with no evidence of medical problems

Exclusion Criteria:

  • Smoking
  • Anemia

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT03569163

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United States, California
UCSF Hypoxia Lab
San Francisco, California, United States, 94143
Sponsors and Collaborators
Spry Health
University of California, San Francisco

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Responsible Party: Spry Health Identifier: NCT03569163     History of Changes
Other Study ID Numbers: SpryHealth
First Posted: June 26, 2018    Key Record Dates
Last Update Posted: June 26, 2018
Last Verified: June 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: Yes
Device Product Not Approved or Cleared by U.S. FDA: Yes
Product Manufactured in and Exported from the U.S.: No
Additional relevant MeSH terms:
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Signs and Symptoms, Respiratory
Signs and Symptoms