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Not Yet RecruitingNCT05711329

Comparison of Methodology Proposed by the SFAR for the Detection by Videoconference of Obstructive Sleep Apnea.

The Aim of This Study is to Determine the Accuracy of the Self-reported Parameters (Compared to Measurement Performed by the Physician) and the Influence of OSA Screening Scores.

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
210 (estimated)
Sponsor
Astes · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The SFAR (French society of anesthesiology and ICU) proposed a method to detect OSA (Obstructive Sleep Apnea) patients via videoconference. The aim of this study is to compare the result of this method with the results of polysomnography (PSG) which remains the gold standard in the detection of OSA patients.

Detailed description

The SFAR (French society of anesthesiology and ICU) proposed a method to detect OSA (Obstructive Sleep Apnea) patients via videoconference. The aim of this study is to compare the result of this method with the results of polysomnography (PSG) which remains the gold standard in the detection of OSA patients. Other methods, such as a predictive score, also exist. The accuracy of the French method compared to PSG and the predictive scores is to be determined.

Conditions

Interventions

TypeNameDescription
OTHERAccuracyWe will validate the accuracy of the method proposed by the SFAR to detect OSA patients via videoconference (in comparison with the results of the PSG).

Timeline

Start date
2024-11-01
Primary completion
2025-09-30
Completion
2025-12-31
First posted
2023-02-03
Last updated
2024-04-23

Source: ClinicalTrials.gov record NCT05711329. Inclusion in this directory is not an endorsement.