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Functionality of the Pulse Oximeter and Accelerometer Portions of a Novel Wearable Device

NCT05197790 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 27

Last updated 2026-03-17

Study results available
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Summary

The purpose of this study is to asses the function of an oxygen sensor and the movement sensor in a novel device prototype.

Conditions

  • Hypoxic Events

Interventions

DEVICE

FDA approved pulse oximeter and DOVE device prototype

The objective is to assess reasonable detection of hypoxic episodes

Sponsors & Collaborators

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-05-20
Primary Completion
2024-12-21
Completion
2024-12-28
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05197790 on ClinicalTrials.gov