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Effect of preoperative dexmedetomidine nasal spray on perioperative sleep in patients with insomnia

Effect of preoperative dexmedetomidine nasal spray on perioperative sleep in patients with insomnia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069220
Enrollment
Unknown
Registered
2023-03-09
Start date
2023-03-10
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

insomnia

Interventions

Dextrmetomidine group (group D):Use dexmedetomidine nasal spray before operation
Placebo group (group C):Preoperative use of saline nasal spray

Sponsors

The First Affiliated Hospital of Shihezi University Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-64 years; 2. Meet the diagnostic criteria of insomnia in the International Classification of Sleep Disorders Third edition (ICSD-3); 3. No recent symptoms of respiratory tract infection (within two weeks); 4. Able to cooperate with the evaluation of various scoring scales.

Exclusion criteria

Exclusion criteria: 1. Secondary insomnia caused by symptoms of physical disease or mental disorder; 2. Complicated with serious diseases of important organ functions (such as heart, brain, liver and kidney); 3. Patients who refuse or are allergic to dexmedetomidine; 4. Patients with a history of nasal diseases; 5. History of long-term use of hypnotic drugs (recent 1 month); 6. Pregnant and lactating patients; 7. Complicated sinus syndrome, severe bradycardia (<50 beats/min) or more than second degree atrioventricular block.

Design outcomes

Primary

MeasureTime frame
Sleep efficiency;

Secondary

MeasureTime frame
Sleep latency;Sleep staging;Sleep scale;Hemodynamic indexes;

Countries

China

Contacts

Public ContactLi Yan

The First Affiliated Hospital of Shihezi University Medical College

1249623003@qq.com+86 136 3993 5315

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026