Actively Recruiting

Age: 18Years +
All Genders
NCT04179188

Impact of Bariatric Surgery in Obese Patients With and Without Obstructive Sleep Apnea Syndrome

Led by Ramsay Générale de Santé · Updated on 2019-11-27

400

Participants Needed

1

Research Sites

346 weeks

Total Duration

On this page

Sponsors

R

Ramsay Générale de Santé

Lead Sponsor

D

Dr CODRON

Collaborating Sponsor

AI-Summary

What this Trial Is About

It has been shown to date that obesity is associated with increased mortality and that weight loss significantly improves cardiovascular risk factors. Among patients receiving bariatric surgery, 30-90% have moderate to severe obstructive sleep apnea (OSA) syndrome. Given the strong associations between OSA and cardiometabolic comorbidities, this project is based on the hypothesis of a lower improvement of cardiovascular risk factors and a higher number of post-surgical complications in OSAS patients.

CONDITIONS

Official Title

Impact of Bariatric Surgery in Obese Patients With and Without Obstructive Sleep Apnea Syndrome

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient, male or female, aged over 18
  • Preparing for bariatric surgery (ring, sleeve gastrectomy, or bypass) at the CELIOBE center
  • Affiliated with social security or beneficiary of such a scheme
  • Signed free and informed consent
Not Eligible

You will not qualify if you...

  • Previous bariatric surgery (ring, sleeve gastrectomy, or bypass)
  • Currently receiving CPAP treatment for sleep apnea syndrome
  • Diagnosed with heart failure with altered ejection fraction requiring CPAP in self-guided mode for OSA
  • Considered unlikely to cooperate or follow study requirements
  • Mental illness preventing informed consent collection
  • Under legal protection (guardianship, curatorship, or deprived of liberty by judicial or administrative decision)
  • Pregnant, lactating, or recently gave birth
  • Hospitalized without consent

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

Hôpital privé La Louvière

Lille, Haut de France, France, 59800

Actively Recruiting

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Research Team

J

Jean-François OUDET

CONTACT

M

Marie Barba

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

2

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