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 aged between 18 and 70 years old
- People who have been diagnosed with obstructive sleep apnea (a condition where breathing repeatedly stops during sleep) through an overnight sleep study, either with a moderate level of breathing disruptions plus symptoms such as daytime sleepiness, waking up gasping, or a partner who has noticed snoring or breathing pauses, or with a higher level of breathing disruptions even without symptoms
- People whose blood pressure falls into one of these categories: slightly elevated blood pressure (120–139/80–89 mmHg) with no more than 2 heart or blood vessel risk factors; newly diagnosed higher blood pressure (140–159/90–99 mmHg) with no heart or blood vessel risk factors; currently on stable blood pressure medication but blood pressure has not yet reached normal levels at a low-risk level; or any person without high cardiovascular risk who is willing to try three months of CPAP treatment and attend follow-up appointments (confirm with trial site)
- People who are able to wear a blood pressure monitor for 24 hours and a continuous blood pressure monitoring device
Who may not be able to join:
- People who have already been diagnosed with sleep apnea and are currently receiving treatment for it, such as CPAP, a dental device, or surgery
- People whose high blood pressure is caused by another medical condition unrelated to sleep apnea, such as kidney artery narrowing, kidney disease, Cushing's syndrome, or a hormone-producing condition called primary aldosteronism
- People who have had a heart attack, stroke, or major surgery in the past 3 months, or who have severe daytime sleepiness, significant memory or thinking problems, active mental illness, or problems with drug or alcohol use
- People with rheumatic or immune system diseases, or with cancer
- People with diseases affecting the large blood vessels, such as giant cell arteritis, a tear in an artery wall, or an aneurysm
- People with conditions that make blood pressure readings unreliable, such as an irregular heartbeat (atrial fibrillation) or blood vessel disease in the arms
- People with a specific inherited form of high blood pressure that begins at a young age (early-onset familial hypertension)
- People who have used any prescription or over-the-counter sleep aid in the four weeks before joining, including medications such as benzodiazepines, zopiclone-type drugs, melatonin-based medications, trazodone, or sedating antidepressants or antihistamines
- People who are allergic to or medically unable to take trazodone or zopiclone, which are potential study medications
- People who are pregnant, breastfeeding, or planning to become pregnant
- People who regularly work night shifts three or more nights per week, or who have been diagnosed by a doctor with a circadian rhythm (body clock) disorder
- People who are already taking part in another clinical trial that involves a treatment or intervention
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
Phone: +86 010-64456527
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
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Trial details
Where this trial is recruiting
Primary endpoints
blood pressure
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Data last synced from ClinicalTrials.gov: 7 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.