Sleep Disorders Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with obstructive sleep apnea (OSA), whether or not they are currently being treated for it, and who are scheduled for planned (non-emergency) surgery at the AUMC operating theatres with an expected hospital stay of at least 3 nights
- People who use a CPAP machine or a mandibular advancement device (a mouthguard-type device worn during sleep) are considered to have treatment for OSA and may be eligible
- People aged 18 years or older
- People who speak Dutch or English
- People who are willing and able to give written consent for their medical care data to be used for research purposes
Who may not be able to join:
- People under 18 years of age
- People who do not speak Dutch or English
- People who do not give consent for their medical care data to be used for research purposes
- People whose surgery is scheduled as a same-day procedure, or whose expected discharge from hospital is before the third night after surgery
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Jeroen Hermanides, Prof. Dr., AmsterdamUMC
Phone: +31205669111
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
AHI and Desaturations on night one and three after surgery
Can't join this trial?
Data last synced from ClinicalTrials.gov: 9 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.