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NightOwl SpO2 Calibration Study

NCT04194073 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2019-12-11

No results posted yet for this study

Summary

Calibration of a software module that computes Oxygen saturation(SpO2) based on photoplethysmography (PPG) traces acquired by the NightOwl reflectance-based PPG sensor which is placed on the finger.

The study is designed in accordance with Medical electrical equipment - Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment (ISO 80601- 2-61:2011)

Conditions

  • Pulse Oximeter Calibration

Interventions

DEVICE

Pulse oximeter calibration population (NightOwl)

The NightOwl is a finger and/or forehead mounted device with, among other functions, the capability to acquire double-wavelength PPG, from which SpO2 can be derived

Sponsors & Collaborators

  • Ectosense NV

    lead INDUSTRY

Principal Investigators

  • Raf De Jongh, MD PhD · Ziekenhuis Oost-Limburg

Study Design

Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-12-07
Primary Completion
2020-01-31
Completion
2020-01-31

Countries

  • Belgium

Study Locations

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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 NCT04194073 on ClinicalTrials.gov