Effectiveness of VistaO2 Device in Screening of Sleep Apnea/Hypopnea Syndrome
NCT ID: NCT01135303
Last Updated: 2011-07-21
Study Results
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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COMPLETED
NA
182 participants
INTERVENTIONAL
2009-02-28
2011-01-31
Brief Summary
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In this context, early detection of such a disease is crucial if the management is tailored to the patient, the practitioner's choice of therapy moving towards continuous positive airway pressure (CPAP) or mandibular advancement device. The detection is based on full nocturnal polysomnography or polygraphic recordings. Polysomnography remains the gold standard but it is a time consuming and costly examination. Polygraphic recording is a test that allows simplified the diagnosis of severe patients, but may not be sufficient for mild form of SAHS. Thus, the SAHS is a pathology under-diagnosed and under-treated. The validation of a technique for identifying patients most at risk to either limit the number of polysomnographic examination is requested.
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Detailed Description
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Analysis of heart rate variability (HRV) has already shown interest in screening SAHS. We therefore wish to evaluate the performance of the analysis of data from the screening tool VistaO2 face what the gold standard synchronized polysomnography.
Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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VistaO2 device
This device combines the transcutaneous oxyhemoglobin saturation (allowing to compute the oxyhemoglobin desaturation index), the slow variations in heart rate and an index of nocturnal respiratory events calculated by analyzing the movements of the chest performed by chest impedance variations.
VistaO2 device
Full night VistaO2 device monitoring synchronized with the gold standard polysomnography.
Interventions
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VistaO2 device
Full night VistaO2 device monitoring synchronized with the gold standard polysomnography.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* written consent
Exclusion Criteria
* diabetes
* atrial fibrillation
* electrode allergy
18 Years
80 Years
ALL
No
Sponsors
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Novacor
UNKNOWN
Centre Hospitalier Universitaire de Saint Etienne
OTHER
Responsible Party
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Centre Hospitalier Universitaire de Saint-Etienne
Principal Investigators
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Frédéric ROCHE, MD-PhD
Role: PRINCIPAL_INVESTIGATOR
CHU de Saint-Etienne
Locations
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Hôpital TENON - APHP
Paris, , France
CHU de Saint-Etienne
Saint-Etienne, , France
Countries
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References
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Chouchou F, Poupard L, Philippe C, Court-Fortune I, Barthelemy JC, Roche F. Thoracic impedance, in association with oximetry, in a multi-modal ECG Holter system is useful for screening sleep disordered breathing. Int J Cardiol. 2013 Feb 10;163(1):100-2. doi: 10.1016/j.ijcard.2012.06.082. Epub 2012 Jul 16. No abstract available.
Other Identifiers
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2008-A01530-55
Identifier Type: OTHER
Identifier Source: secondary_id
0808119
Identifier Type: -
Identifier Source: org_study_id
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