Sleep Disorders Trial, Recruiting NCT07357272 Sponsor: Beijing Anzhen Hospital Condition: Sleep Disorders
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Sleep Disorders Trial, Recruiting

NCT07357272
Recruiting Not Applicable

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 7 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Beijing Anzhen Hospital
Registry
ClinicalTrials.gov
Start date
15 September 2025
Est. completion
1 July 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

blood pressure

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov