Status:

COMPLETED

Predictability of OSA With a Subjective Screening Scale (OSASSS1)

Lead Sponsor:

Center for Sleep Medicine - Clinique André Renard

Collaborating Sponsors:

PIRON Alain, Osteopath - physiotherapist

LACROIX Alain, neurologist, MD, PhD

Conditions:

Obstructive Sleep Apnea

OSA

Eligibility:

All Genders

18-77 years

Brief Summary

the study aims to evaluate the accuracy correlation between subjective perception of the air flow through airways from patients and survey and/or polysomnography they spent, using a brief clinical pro...

Detailed Description

The subjects in the study are 18 to 77 years old and present the following conditions: * polysomnography and sleep survey realized at the Center for Sleep Medicine André RENARD, without any informati...

Eligibility Criteria

Inclusion

  • Female or male subjects aged 18 to 77 years old
  • subjects who have performed a PSG at the sleep medicine center André Renard for the study group
  • subjects with no sleep disorder on sleep survey for the control group
  • Subjects who agree to comply with the requirements of the study.
  • Subjects who are of age (and know how to read and write) who have given their informed, explicit consent in advance to any procedure related to the trial, the study or the investigation conducted on human beings, with the objective of developing knowledge specific to the exercise of health care professions, as set out in Royal Decree No. 78 of 10 November 1967 on the practice of the health care professions (Act of 27 December 2005)

Exclusion

  • subjects with acute infections
  • subjects with trauma within the last 72 hours
  • subjects who already benefit from OSA treatment
  • subjects with known perceptual disorders, for example post-stroke
  • subjects with current or recent chemotherapy and radiotherapy treatment
  • Pregnant women
  • Criteria related to prior or concurrent treatments:
  • Treatment with antipsychotics, anxiolytics, soporifics or muscle relaxants started within the two months preceding the study.
  • Treatment with intraoral implants during the study or in the two months preceding the study

Key Trial Info

Start Date :

January 1 2023

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

November 30 2024

Estimated Enrollment :

112 Patients enrolled

Trial Details

Trial ID

NCT06092710

Start Date

January 1 2023

End Date

November 30 2024

Last Update

June 3 2025

Active Locations (1)

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Centre de médecine du sommeil- Clinique André Renard

Herstal, Liège, Belgium, 4040