Eyelid Movement Sensor Device- Blinking Characterizing

NCT ID: NCT02309814

Last Updated: 2016-09-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-01-31

Study Completion Date

2016-08-31

Brief Summary

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The investigators have developed a simple to use device that facilitates the monitoring of the upper eyelids motion, acquires the eyelid vertical movement and enables analysis and graphic presentation of the results. the device system consists 3 components : glasses for the patient including magneto sensitive probes, hardware and dedicated software.

Our purpose is to characterize eyelid motion in normal population. The methods include measuring each patient 10 minutes during watching a short movie.

Detailed Description

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Essentially, for Hall-probes monitor the magnetic field generated by a tiny magnets attached to the upper eyelid.

Conditions

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Eyelid Movement Disorders

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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eyelid motion sensor device

all volunteers will wear the monitor eyelid sensor device (including the tiny magnets on the upper eyelid). a 10 minutes movie will be screened on 40 inch television screen in a 3 meters distance.

Group Type EXPERIMENTAL

eyelid motion sensor device (Hall-probe)

Intervention Type DEVICE

all volunteers will wear the eyelid motion sensor device (Hall-probe) (including the tiny magnets on the upper eyelid). a 10 minutes movie will be screened on 40 inch television screen in a 3 meters distance

Interventions

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eyelid motion sensor device (Hall-probe)

all volunteers will wear the eyelid motion sensor device (Hall-probe) (including the tiny magnets on the upper eyelid). a 10 minutes movie will be screened on 40 inch television screen in a 3 meters distance

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* healthy 18-67 year olds with no eye medical history

Exclusion Criteria

* pregnancy
* head trauma history
* using contact lens
Minimum Eligible Age

18 Years

Maximum Eligible Age

67 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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HaEmek Medical Center, Israel

OTHER

Sponsor Role lead

Responsible Party

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daniel briscoe

Head of ophthalmology departement

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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daniel briscoe

Role: PRINCIPAL_INVESTIGATOR

haemek medical center

Other Identifiers

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0133-13-EMC

Identifier Type: -

Identifier Source: org_study_id

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