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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03047941 |
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Date of registration:
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06/02/2017 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Determination of Optimal Cutoff Value for Screening Severe Hypoxemic OSA (Obstructive Sleep Apnea) Patients
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Scientific title:
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Determination of Optimal Cutoff Value of 4 Tests (DES-OSA, STOP-Bang, OSA50, P-SAP) for Screening Severe Hypoxemic OSA (Obstructive Sleep Apnea) Patients |
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Date of first enrolment:
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February 13, 2017 |
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Target sample size:
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0 |
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Recruitment status: |
Withdrawn |
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URL:
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https://clinicaltrials.gov/show/NCT03047941 |
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Study type:
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Observational [Patient Registry] |
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Study design:
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Phase:
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Countries of recruitment
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Belgium
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- All patients scheduled to have a PSG in the sleep laboratory center.
Exclusion Criteria:
- Patients < 18 years
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Sleep Apnea, Obstructive
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Intervention(s)
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Diagnostic Test: Determination of optimal cutoff values.
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Primary Outcome(s)
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Adequacy of STOP-Bang to detect severe hypoxemic OSA patients
[Time Frame: One week.]
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Adequacy of OSA50 to detect severe hypoxemic OSA patients
[Time Frame: One week]
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Adequacy of P-SAP to detect severe hypoxemic OSA patients
[Time Frame: One week]
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Adequacy of DES-OSA to detect severe hypoxemic OSA patients
[Time Frame: One week]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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