Actively Recruiting

Age: 18Years +
All Genders
NCT07283289

Prevalence of Obstructive Sleep Apnea in Patients With Peripheral Arterial Occlusive Disease

Led by Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer · Updated on 2026-04-14

295

Participants Needed

1

Research Sites

51 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Obstructive sleep apnea syndrome (OSAS) is characterized by partial (hypopnea) or complete (apnea) obstruction of the upper airways, leading to intermittent hypoxemia and sleep fragmentation. Peripheral arterial occlusive disease (PAOD) is a chronic condition defined by the narrowing or occlusion of arteries in the lower limbs, often resulting in ischemia of downstream tissues. This disease is a common complication of atherosclerosis and affects approximately 1.2% of the general French population. OSAS is a well-established risk factor for atherosclerotic disease, particularly for coronary and neurovascular events. Although a relationship between OSAS and PAOD has been investigated in recent years, the link has not been definitively established and requires further study. Therefore, this preliminary cohort study aims to observe the prevalence of OSAS among patients diagnosed with PAOD, regardless of the disease stage.

CONDITIONS

Official Title

Prevalence of Obstructive Sleep Apnea in Patients With Peripheral Arterial Occlusive Disease

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Confirmed diagnosis of Peripheral Arterial Occlusive Disease (PAOD), regardless of disease stage or previous surgery
  • No objection to use of pseudonymised medical data
  • Sleep polygraphy scheduled as part of routine care within one month
Not Eligible

You will not qualify if you...

  • Unable to perform Ankle-Brachial Index or sleep polygraphy due to physical or cognitive limitations
  • Previous diagnosis of Obstructive Sleep Apnea Syndrome (OSAS) confirmed by polygraphy and currently treated with nocturnal therapy such as CPAP

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Centre Hospitalier Intercommunal Toulon La Seyne sur Mer

Toulon, Var, France, 83056

Actively Recruiting

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Research Team

L

Léonie GEY, M.D.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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