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Comparison of Different Screening Score for Hypoxemic OSA (Obstructive Sleep Apnea) With the Results of a Polysomnography (PSG)

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ClinicalTrials.gov Identifier: NCT02050685
Recruitment Status : Completed
First Posted : January 31, 2014
Last Update Posted : January 6, 2016
Sponsor:
Information provided by (Responsible Party):
Eric DEFLANDRE, MD, FCCP, Astes

Brief Summary:
Comparison of different screening score for hypoxemic OSA (Obstructive Sleep Apnea) with the results of a polysomnography (PSG). The different screening score studied are: STOP-BANG, DES-OSA, P-SAP and OSA50.

Condition or disease Intervention/treatment
Sleep Apnea, Obstructive Other: All patients incoming in the sleep study centre for a PSG

Detailed Description:
The investigators should compare the four screening scores (STOP-BANG, DES-OSA, P-SAP and OSA50) with the results of the PSG (and in particular the number of apnea and hypopnea index and the probability of hypoxemia).

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Study Type : Observational
Actual Enrollment : 159 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Comparison of Different Screening Score for Hypoxemic OSA
Study Start Date : January 2014
Actual Primary Completion Date : December 2015
Actual Study Completion Date : December 2015

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Sleep Apnea

Group/Cohort Intervention/treatment
All patients for PSG at SLBO
All patients incoming in the sleep study centre for a PSG. At the arrival the screening score will be recorder. AHI will be recorded next morning after analysis of the PSG.
Other: All patients incoming in the sleep study centre for a PSG
All patients incoming in the sleep study centre for a PSG. Comparison between screening score and AHI derived from PSG.




Primary Outcome Measures :
  1. Comparison of the DES-OSA score with previously described scores. [ Time Frame: The day before the PSG (PolySomnoGraphy) ]
    Comparison of the DES-OSA score with the results of previously described scores (STOP-BANG, P-SAP and OSA50).


Secondary Outcome Measures :
  1. Comparison of the four screening scores with results of the PSG. [ Time Frame: The day after the polysomnography ]
    Comparison of the four screening scores collected past day (before PSG - PolySomnoGraphy) with the results of the PSG (especially the AHI: Apnea Hypopnea Index)



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
All adults patients for an overnight polysomnography at SLBO.
Criteria

Inclusion Criteria:

  • Adults patients (> 18 years)

Exclusion Criteria:

  • None

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02050685


Locations
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Belgium
Clinique Saint-Luc de Bouge
Bouge, Namur, Belgium, 5004
Sponsors and Collaborators
Eric DEFLANDRE, MD, FCCP
Investigators
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Principal Investigator: Eric P DEFLANDRE, MD, FCCP Astes

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Eric DEFLANDRE, MD, FCCP, ERIC DEFLANDRE, MD, FCCP, Astes
ClinicalTrials.gov Identifier: NCT02050685     History of Changes
Other Study ID Numbers: REES-ASTES-2014
First Posted: January 31, 2014    Key Record Dates
Last Update Posted: January 6, 2016
Last Verified: January 2016

Additional relevant MeSH terms:
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Sleep Apnea Syndromes
Sleep Apnea, Obstructive
Apnea
Respiration Disorders
Respiratory Tract Diseases
Sleep Disorders, Intrinsic
Dyssomnias
Sleep Wake Disorders
Nervous System Diseases