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Clinical Trial Summary

Additional data on screening for obstructive sleep apnea/hypopnea syndrome (OSAHS) in patients with co-morbidities, such as diabetics and those with chronic respiratory diseases would enable current recommendations to evolve, with a view to promoting the widespread use of simplified techniques for OSAHS screening, particularly in patients with cardiorespiratory co-morbidities. The primary objective of this observational multicentric pilot study is to compare the performance of the Sunrise® medical device with that of ventilatory polygraphy as part of routine screening for OSAHS in diabetic patients followed up in the diabetology department of the Strasbourg University Hospital, and in patients followed up in the pneumology consultation department of Mulhouse Hospital (GHRMSA).


Clinical Trial Description

Secondary objectives 1. To assess the correlation of the following parameters: - dorsal Apnea-Hypopnea Index (AHI) measured by ventilatory polygraphy and dorsal Obstructive Respiratory Disturbance Index (ORDI) measured by Sunrise® device - non-dorsal AHI measured by ventilatory polygraphy and non-dorsal ORDI measured by Sunrise® device 2. To study the correlation between AHI measured by the Sunrise® medical device and desaturation index measured by ventilatory polygraphy. Conduct of research - At Strasbourg University Hospital, the study will be proposed to patients admitted for diabetic assessment who require ventilatory polygraphy. - At Mulhouse hospital (GHRMSA), patients are referred to a pneumologist in case of suspected OSAHS and a ventilatory polygraphy is scheduled at home. Patients scheduled to undergo this examination will be invited to take part in the study. Ventilatory polygraphy (routine care): Patients included in the study will receive an additional recording using the Sunrise© medical device, performed simultaneously with the ventilatory polygraphy. Ventilatory polygraphy will be performed in accordance with each center's usual practices. For patients undergoing home polygraphy (GHRMSA), the care team will install the sensors and program the device for recording during sleep. The patient will return home and spend the night there, before coming back to the hospital the following day to give back the equipment. For patients hospitalized in the diabetology department of Strasbourg University Hospital, ventilatory polygraphy will be carried out during hospitalization. Sunrise© medical device (examination added by research): The mobile application will be installed on patient's smartphone by the study investigating team, and the use of the Sunrise© device will be explained to the patient. Recording will take place on the same night as the ventilatory polygraphy. The day after recording, the Sunrise© sensor and ventilatory polygraph equipment will be collected by the investigating team. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06460441
Study type Observational
Source Groupe Hospitalier de la Region de Mulhouse et Sud Alsace
Contact
Status Not yet recruiting
Phase
Start date June 17, 2024
Completion date December 17, 2024

See also
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