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Evaluation of the Ear-EEG System for Sleep Monitoring in Healthy Subjects

NCT03586310 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2020-11-12

No results posted yet for this study

Summary

Subjects sleep multiple nights in their own home, wearing actigraph, PSG (PolySomnoGraphy) and ear-EEG sensors. The object of the study is to determine the applicability of ear-EEG for sleep monitoring.

Conditions

  • Sleep Monitoring

Interventions

DEVICE

ear-EEG

soft silicone electrode array placed in each ear (outer ear-canal and concha), connected to a battery powered EEG amplifier.

Sponsors & Collaborators

  • Uneeg medical

    collaborator UNKNOWN

  • University of Aarhus

    lead OTHER

Principal Investigators

  • Preben Kidmose, Professor · University of Aarhus

Study Design

Allocation
NON_RANDOMIZED
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2018-03-23
Primary Completion
2020-11-09
Completion
2020-11-09

Countries

  • Denmark

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 NCT03586310 on ClinicalTrials.gov