Home Monitoring for Suspected Obstructive Sleep Apnea

Variability in Nocturnal Oxygen Parameters in Suspected Obstructive Sleep Apnea (OSA)

Recruiting N/A Interventional Study
Obstructive Sleep Apnea
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
130 (estimated)
Sponsor
Universitaire Ziekenhuizen KU Leuven · Other
Who this trial is looking for

This trial is looking for people who might have obstructive sleep apnea and need a sleep test. Participants will monitor their oxygen levels at home for 7 nights and spend 1 night at a hospital for a more detailed assessment.

Are You a Good Fit for This Trial?

You may be able to join if

  • I have suspected obstructive sleep apnea and need a sleep test.

You may not be able to join if

  • I am younger than 18 years old.
  • I cannot read or understand the consent form.
  • I have a neuromuscular disease.
  • I have a chest wall disease that causes breathing problems.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial

The investigators would like to evaluate the variability of oxygen (and PPG) parameters during 7 nights at home. Oxygen (and PPG) parameters will also be evaluated during 1 night at the hospital (diagnostic polysomnography). Based on currently developed algorithms, surrogate apnea-hypopnea index (AHI), cardiovascular status and the variability of these parameters will be evaluated.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients with suspected OSA with a clinical indication to perform a polysomnography Exclusion Criteria: * Patients younger than 18 yrs * Patients not able to read or understand the informed consent content on the purpose of the study, due to visual, intellectual or language …
Contacts

Bertien Buyse, MD, PhD

+32 16 342522

Bertien.Buyse@uzleuven.be

CONTACT

Dries Testelmans, MD, PhD

+32 16 342522

Dries.Testelmans@uzleuven.be

CONTACT