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Clinical study of self-controlled sleep regulation based on dexmedetomidine in improving postoperative sleep disorder

Clinical study of self-controlled sleep regulation based on dexmedetomidine in improving postoperative sleep disorder

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071710
Enrollment
Unknown
Registered
2023-05-23
Start date
2023-05-25
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Postoperative sleep disorder

Interventions

Experimental group:After operation, dexmetomidine was pumped into the self-controlled drug delivery device
Control group:After operation, normal saline was pumped into the automatic drug delivery device

Sponsors

Department of Anesthesiology, Changzhou Second People's Hosptial Affiliated to Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients who need surgical treatment for gastrointestinal tumors (colon cancer, gastric cancer); 2. ASA grade I-II level; 3. Pittsburgh sleep score is less than 7 before operation and >= 7 after operation.

Exclusion criteria

Exclusion criteria: 1. Those who have a history of gastrointestinal surgery; 2. Nervous system diseases, mental disorders, language disorders, cognitive disorders or other diseases that affect the quality of sleep; 3. Patients with history of other malignant tumors; 4. Patients with severe heart, liver, lung and kidney dysfunction.

Design outcomes

Primary

MeasureTime frame
Non-REM sleep time;REM sleep time;Depression score;

Secondary

MeasureTime frame
VAS score;Score of quality of life recovery scale;Serum inflammatory factor;

Countries

China

Contacts

Public ContactZhouquan Wu

The Second People's Hospital of Changzhou, Jiangsu

151897127@qq.com+86 138 6102 3270

Outcome results

None listed

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