- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02051829
Comparison of Preoperative Screening Score for Obstructive Sleep Apnea (OSA)
April 21, 2016 updated by: Eric DEFLANDRE, MD, FCCP, Astes
Comparison of Preoperative Screening Score for OSA
Comparison of preoperative screening score for OSA.
In a preoperative population, comparison of the STOP-BANG, DES-OSA, P-SAP and OSA50 score.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Comparison of preoperative screening score for OSA (Obstructive Sleep Apnea). In a preoperative population, comparison of the STOP-BANG, DES-OSA, P-SAP and OSA50 score.
Comparison between scores and if applied with the results of a polysomnography (PSG).
Study Type
Observational
Enrollment (Actual)
1584
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Jambes, Belgium, 5100
- Cabinet Medical ASTES
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Adult patients (> 18 years) presenting for preoperative assessment before surgery at SLBO.
Description
Inclusion Criteria:
- All adults patients (> 18 years) performing a preoperative assessment at the ASTES Doctor's Office (ASTES is an acronym with the name of Medical Doctors involved in this office)
Exclusion Criteria:
- Patients < 18 years
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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All patients
Comparison of the four screening score
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Comparison of the four screening score, for patient making a preoperative assessment for SLBO (clinique Saint-Luc de BOuge)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Number of patients with a positive DES-OSA score
Time Frame: Baseline
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Comparison of the result of the DES-OSA score with results of previously describes scores (STOP-BANG, OSA50 and P-SAP).
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Baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of patients with a positive STOP-Bang score and a positive PSG (PolySomnoGraphy)
Time Frame: Baseline
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For the patients with a positive STOP-Bang score: we will make a PSG.
After this one, we will compare the result of four scores (STOP-Bang, OSA50, P-SAP and DES-OSA) and the result of the PSG (especially AHI: Apnea Hypopnea Index)
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Baseline
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2014
Primary Completion (Actual)
April 1, 2016
Study Completion (Actual)
April 1, 2016
Study Registration Dates
First Submitted
January 24, 2014
First Submitted That Met QC Criteria
January 30, 2014
First Posted (Estimate)
January 31, 2014
Study Record Updates
Last Update Posted (Estimate)
April 22, 2016
Last Update Submitted That Met QC Criteria
April 21, 2016
Last Verified
April 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SEED-ASTES-2014
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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