Actively Recruiting
The SNORE-trial: Analysis of Alterations in Sleep Stages Following Anesthesia and Their Relation to the Severity of Obstructive Sleep Apnea in the First 3 Nights After Surgery
Led by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Updated on 2025-01-29
35
Participants Needed
2
Research Sites
43 weeks
Total Duration
On this page
Sponsors
A
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Lead Sponsor
V
VU University of Amsterdam
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this observational study is to learn about the relationship between sleep alterations following anesthesia and their relationship to a potential increase of obstructive sleep apnea (OSA) severity. Our main question is: Is there an increased severity of OSA on the third post-operative night compared to the first post-operative night and does this have a relation with REM sleep? Participants enrolled in this research are all diagnosed with OSA, with or without treament. All participants will be asked to wear a watchlike device called WATCHPAT to identify sleep paterns and register apneic (no breathing) and hypopneic (insufficient breathing) incidents. We ask our participants to wear this device for 8-10 hours a night when they are a sleep.
CONDITIONS
Official Title
The SNORE-trial: Analysis of Alterations in Sleep Stages Following Anesthesia and Their Relation to the Severity of Obstructive Sleep Apnea in the First 3 Nights After Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients scheduled for elective surgery at the AUMC with a diagnosis of OSA with or without treatment and expected hospital stay of at least 3 days
- Patients treated with continuous positive airway pressure (CPAP) or mandibular advancement device (MAD) are included
- Patients 18 years or older
- Dutch or English speaking
- Willing and able to sign consent for re-use of care data
You will not qualify if you...
- Patients under 18 years old
- Patients not speaking Dutch or English
- Patients who do not sign consent for re-use of care data
- Surgery scheduled as day case or with expected discharge before the third night after surgery
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
AmsterdamUMC, location AMC
Amsterdam, North Holland, Netherlands, 1105 AZ
Actively Recruiting
2
Amsterdam UMC location VuMC
Amsterdam, Netherlands, 1081 HV
Actively Recruiting
Research Team
M
Martin V.H. Rutten, Msc, MD
CONTACT
J
Jeroen Hermanides, Prof. Dr.
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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