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DexmedetOmidine Complement Treats Chronic insOmnia and Improves Circadian Rhythm (DOCTOR)

Key facts

Who runs it
Ruijin Hospital
Where
China1 site in 1 countryChoose a country to see its sites
Trial code
Status
Completed
People taking part
64 people enrolled
Started
14 May 2021
Ended
7 Mar 2024
Type of study
Interventional, 2 groupsOne group gets a placebo (a dummy treatment), for comparison.
Treatments tested
  • dexmedetomidine
  • saline
Record updated
15 January 2025

Who can take part

Age
18 years to 65 years
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 8 criteriaShow less

Who can take part

  • Age between 18- 65 years old
  • Body mass index (BMI) between 18 and 35 kg/m\^2;
  • Clinical diagnosis of chronic insomnia;
  • Must be able to communicate with site personnel

Who cannot take part

  • Current use of psychotropic drug
  • Clinical diagnosis of mental disorders
  • Clinical diagnosis of neurological diseases
  • Pregnancy

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

About the trial

What the trial wants to find out

It has been reported that dexmedetomidine, alpha-2 adrenoceptor agonist, can activate endogenous neural sleep pathways in the central nervous system. This randomised, double-blinded and controlled trial was designed to investigate whether dexmedetomidine can improve/treat chronic insomnia patients. Its effects on sleep quality and improvement, EEG and circadian rhythm, brain connectivity, cognition and biomarker changes are determined.

The 2 groups in the trial

  • dexmedetomidineTreatment being tested

    0.5μg/kg bolus injection in 10 minutes followed by 0.1µg/kg/hr pump infusion from 23:30 pm to 6:30 am

  • salinePlacebo, for comparison

    the same rate as dexmedetomidine

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
The Effect of Dexmedetomidine on Patients With Chronic Insomnia and Its Influence on Circadian Rhythm:Randomized Clinical Trial, Double Blind
Record updated
15 January 2025