Condition: Sleep Apnea Syndrome, Obstructive · Sleep Apnea Syndrome (OSAS) · Sponsor: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
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.
This description comes directly from the study's public registry record.
Martin V.H. Rutten, Msc, MD · +31205669111 · m.v.rutten@amsterdamumc.nl
Jeroen Hermanides, Prof. Dr. · +310205669111 · j.hermanides@amsterdamumc.nl
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| AmsterdamUMC, location AMC | Amsterdam, North Holland, Netherlands | Recruiting |
| Amsterdam UMC location VuMC | Amsterdam, Netherlands | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06586268