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Real-time Attended Home-polysomnography Through Telematic Data Transmission

NCT ID: NCT01471626

Last Updated: 2012-10-05

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

21 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-12-31

Study Completion Date

2012-03-31

Brief Summary

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The purpose of this study is to develop an efficient home-based polysomnography device, which allows, through GPRS,continuous real-time monitoring from the sleep lab based in the hospital, in order to decrease the failure rate of home-based recordings.

Detailed Description

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Conditions

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Obstructive Sleep Apnea

Keywords

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sleep apnea polysomnography telemedicine

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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telematic attended polysomnography

Group Type EXPERIMENTAL

polysomnograph Dream and Sleep Box

Intervention Type DEVICE

Portable polysomnograph will be placed at home around 7:00PM. The Sleep Box (wireless monitoring device) will be left near the patient, to allow real-time GPRS transmission of recorded sleep parameters to the sleep lab.

Interventions

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polysomnograph Dream and Sleep Box

Portable polysomnograph will be placed at home around 7:00PM. The Sleep Box (wireless monitoring device) will be left near the patient, to allow real-time GPRS transmission of recorded sleep parameters to the sleep lab.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* clinical suspicion of OSA
* 18 y old

Exclusion Criteria

* restrictive respiratory disorders
* distance home-hospital exceeding 30 Km.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire Saint Pierre

OTHER

Sponsor Role lead

Responsible Party

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Marie Bruyneel

pneumologist, chef de clinique adjoint

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Marie Bruyneel, MD

Role: PRINCIPAL_INVESTIGATOR

CHU St Pierre

Locations

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CHU St Pierre

Brussels, , Belgium

Site Status

Countries

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Belgium

Other Identifiers

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AK/-10-81/4077

Identifier Type: -

Identifier Source: org_study_id