Skip to content

Observation and Study on the Sedative-Hypnotic Effects of Dexmedetomidine

Observation and Study on the Sedative-Hypnotic Effects of Dexmedetomidine

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118574
Enrollment
Unknown
Registered
2026-02-09
Start date
2026-03-05
Completion date
Unknown
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Insonmia

Interventions

A group:Intranasal spray of dexmedetomidine
B group:Intravenous injection of dexmedetomidine.

Sponsors

Shanghai Fourth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 18–65 years, male or female. 2. Meets the diagnostic criteria for insomnia according to ICSD-3 or DSM-5. 3. Normal liver and kidney function (within the normal reference range) and no severe arrhythmia on electrocardiogram (ECG). 4. Agreement to participate in the study and provision of signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Diagnosed with a major systemic disease within the past 6 months or currently undergoing treatment for such a condition. 2. History of allergy to dexmedetomidine. 3. Female subjects who are pregnant or lactating. 4. Failure to provide written informed consent, or provision of consent but presence of severe cognitive impairment, language communication barriers, or inability to cooperate with polysomnography (PSG) monitoring as assessed by the investigator. 5. Patients with hepatic or renal insufficiency, bradycardia, or hypotension. 6. A history of alcohol abuse, substance abuse within the past 3 months, or current smokin

Design outcomes

Primary

MeasureTime frame
Sleep Stage;Concentration-time curve;

Secondary

MeasureTime frame
Sleep latency;Total sleep time;Number of arousal;Wake After Sleep Onset;

Countries

Chian

Contacts

Public ContactQifang Li

Shanghai Fourth People‘s Hospital

liqifang2004@126.com+86 136 7183 4019

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026