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Clinical Trials/NCT01471626
NCT01471626CompletedNot Applicable

Real-time Attended Home-polysomnography Through Telematic Data Transmission

Centre Hospitalier Universitaire Saint Pierre1 site in 1 country21 target enrollmentStarted: December 1, 2011Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
21
Locations
1
Primary Endpoint
Quality of Polysomnographic Recordings

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •clinical suspicion of OSA

Exclusion Criteria

  • •restrictive respiratory disorders
  • •distance home-hospital exceeding 30 Km.

Arms & Interventions

telematic attended polysomnography

Experimental

Intervention: polysomnograph Dream and Sleep Box (Device)

Outcomes

Primary Outcomes

Quality of Polysomnographic Recordings

Time Frame: 1 week

Quality of recordings will be graded according to Redline S et al (SLEEP 1998): Unsatisfactory, poor, fair, good, very good,excellent. Unsatisfactory and poor recordings are considered as failures.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Centre Hospitalier Universitaire Saint Pierre
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Marie Bruyneel

pneumologist, chef de clinique adjoint

Centre Hospitalier Universitaire Saint Pierre

Study Sites (1)

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