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 assessed by their doctors as medically suitable for planned (non-emergency) heart bypass surgery (CABG)
- People aged 21 years or older
- People who speak English or Mandarin
- People who are able to give their own consent to participate
Who may not be able to join:
- People who speak languages other than English or Mandarin, as some of the study's assessments require one of these two languages
- People who had a severe hearing impairment, severe cognitive impairment, a progressive neurological condition, or a psychological disorder before their illness or surgery
- People who experience serious surgical complications, including heavy bleeding from surgical sites, severe infection causing the body to shut down that does not respond to maximum treatment, or who are in a critical condition with an expected survival of less than 48 hours
- People who are pregnant
- People who develop delirium (a sudden state of confusion) before the trial treatment has begun
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: Su Ren Wong, National University Hospital, Singapore
Phone: +65-96280613
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
Delirium; Delirium
Can't join this trial?
Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.