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Effectiveness of VistaO2 Device in Screening of Sleep Apnea/Hypopnea Syndrome (VISTAO2)

Primary Purpose

Sleep Apnea Syndromes

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
VistaO2 device
Sponsored by
Centre Hospitalier Universitaire de Saint Etienne
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Sleep Apnea Syndromes focused on measuring Sleep Apnea Syndromes, Polysomnography, Holter ECG, Thoracic impedance, Heart rate variability

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • sleep apnea hypopnea syndrome suspicion
  • written consent

Exclusion Criteria:

  • pacemaker
  • diabetes
  • atrial fibrillation
  • electrode allergy

Sites / Locations

  • Hôpital TENON - APHP
  • CHU de Saint-Etienne

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

VistaO2 device

Arm Description

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.

Outcomes

Primary Outcome Measures

Sleep apnea hypopnea syndrome
Apnea hypopnea index higher than 15, evaluated by polysomnography.

Secondary Outcome Measures

Full Information

First Posted
May 25, 2010
Last Updated
July 20, 2011
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Collaborators
Novacor
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1. Study Identification

Unique Protocol Identification Number
NCT01135303
Brief Title
Effectiveness of VistaO2 Device in Screening of Sleep Apnea/Hypopnea Syndrome
Acronym
VISTAO2
Official Title
Effectiveness of VistaO2 Device in Screening of Sleep Apnea/Hypopnea Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
July 2011
Overall Recruitment Status
Completed
Study Start Date
February 2009 (undefined)
Primary Completion Date
January 2011 (Actual)
Study Completion Date
January 2011 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Collaborators
Novacor

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The high prevalence (9% in men and 4% in women) of sleep apnea / hypopnea syndrome (SAHS) in adults is now well documented as well as its cardiovascular repercussions. Previous studies showed a conclusive link between SAHS and severe cardiovascular diseases such as hypertension, myocardial infarction, heart failure and stroke.Then, SAHS is a public health issue in adults. 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.
Detailed Description
In this perspective, the development of a product screening sleep related breathing disorders for physicians, cardiologists, internists (not specialized sleep experts) would fill this need. It allows for a reliable first screening for their patients in parallel with a routine cardiological examination. Imposing a minimal human and material, the ECG Holter recorder "VistaO2" (NOVACOR, Rueil-Malmaison, France) is a device designed to meet these requirements. This device fits into the daily management of patients with cardiac arrhythmias or sinus/atrioventricular conduction disorders, and of patients suffering myocardial infarction (arrhythmic risk stratification, detection of silent myocardial ischemia). 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Apnea Syndromes
Keywords
Sleep Apnea Syndromes, Polysomnography, Holter ECG, Thoracic impedance, Heart rate variability

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
182 (Actual)

8. Arms, Groups, and Interventions

Arm Title
VistaO2 device
Arm Type
Experimental
Arm Description
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.
Intervention Type
Device
Intervention Name(s)
VistaO2 device
Other Intervention Name(s)
VistaO2 : ECG Holter recorder (Novacor, Rueil-Malmaison, France).
Intervention Description
Full night VistaO2 device monitoring synchronized with the gold standard polysomnography.
Primary Outcome Measure Information:
Title
Sleep apnea hypopnea syndrome
Description
Apnea hypopnea index higher than 15, evaluated by polysomnography.
Time Frame
Day 1

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: sleep apnea hypopnea syndrome suspicion written consent Exclusion Criteria: pacemaker diabetes atrial fibrillation electrode allergy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frédéric ROCHE, MD-PhD
Organizational Affiliation
CHU de Saint-Etienne
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital TENON - APHP
City
Paris
ZIP/Postal Code
75000
Country
France
Facility Name
CHU de Saint-Etienne
City
Saint-etienne
ZIP/Postal Code
42055
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
22805548
Citation
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.
Results Reference
derived

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Effectiveness of VistaO2 Device in Screening of Sleep Apnea/Hypopnea Syndrome

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