Sleep Disorders Trial, Recruiting NCT06376760 Sponsor: Beijing Tiantan Hospital Condition: Sleep Disorders
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Sleep Disorders Trial, Recruiting

NCT06376760
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:

For people with insomnia:

  • Adults aged 18 to 64 years
  • People rated as generally healthy or with only mild health conditions (ASA physical status I–II) (confirm with trial site)
  • People with a body mass index (BMI) between 15 and 30
  • People already scheduled to have a digestive endoscopy procedure using intravenous (IV) sedation
  • People whose sleep difficulties meet the recognised diagnostic criteria for insomnia disorder (DSM-5) (confirm with trial site)
  • People who score 16 or below on a standard sleep quality questionnaire called the Sleep Condition Indicator (a lower score indicates poorer sleep)

For people with normal sleep:

  • Adults aged 18 to 64 years
  • People rated as generally healthy or with only mild health conditions (ASA physical status I–II) (confirm with trial site)
  • People with a BMI between 15 and 30
  • People already scheduled to have a digestive endoscopy procedure using IV sedation
  • People with no history or signs of insomnia

Who may not be able to join:

  • People who have any neurological condition
  • People who drink alcohol every day
  • People who have any medical reason they cannot receive IV anaesthetic drugs, such as very low blood pressure or shock
  • People with a known allergy to any of the medications used in the study
  • People who are pregnant or breastfeeding
  • People who have been diagnosed with sleep apnea
  • People currently experiencing an acute upper respiratory infection (such as a cold or similar illness)
  • People with a psychological condition who are currently experiencing thoughts of suicide
  • People who regularly need to work night shifts or frequently care for children or elderly people during the night

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 26 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Beijing Tiantan Hospital
Registry
ClinicalTrials.gov
Start date
15 April 2024
Est. completion
31 March 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

The total consumption of intravenous anesthetic drug

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: 26 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