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A Single Center Study on the Functionality of the Pulse Oximeter and Accelerometer Portions of a Novel Wearable Device
The purpose of this study is to asses the function of an oxygen sensor and the movement sensor in a novel device prototype.
After informing the patient about the study and the potential risk. The patient is asked to wear a prototype of a novel device to sense oxygen levels and movement for the duration of the visit. The day of the enrolment is when the visit will be completed. The patient is required to complete an overnight sleep test (no more than 15 hrs) with the prototype device worn on their index finger and wrist.
Age
21 - No limit years
Sex
ALL
Healthy Volunteers
No
Hospital of the University of Pennsylvania
Philadelphia, Pennsylvania, United States
Start Date
May 20, 2022
Primary Completion Date
December 21, 2024
Completion Date
December 28, 2024
Last Updated
March 17, 2026
27
ACTUAL participants
FDA approved pulse oximeter and DOVE device prototype
DEVICE
Lead Sponsor
University of Pennsylvania
Data Source & Attribution
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