Actively Recruiting
Variability in Nocturnal Oxygen Parameters in Suspected Obstructive Sleep Apnea (OSA)
Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2024-07-03
130
Participants Needed
1
Research Sites
248 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Variability in Nocturnal Oxygen Parameters in Suspected Obstructive Sleep Apnea (OSA)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with suspected OSA with a clinical indication to perform a polysomnography
You will not qualify if you...
- 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 issues
- Patients with neuromuscular disease or chest wall disease with suspected hypoventilation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University Hospitals Leuven
Leuven, Belgium, 3000
Actively Recruiting
Research Team
B
Bertien Buyse, MD, PhD
CONTACT
D
Dries Testelmans, MD, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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