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A clinical study of perioperative sleep disorders in cardiac surgery patients

A clinical study of perioperative sleep disorders in cardiac surgery patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096037
Enrollment
Unknown
Registered
2025-01-16
Start date
2024-10-11
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

None

Interventions

Group D:Dexmedetomidine infusion 0.3ug/kg/h during anaesthesia
Group E:Infusion of 0.3 mg/kg/h of esketamine during anaesthesia
Group C:Equivalent saline infusion during anaesthesia

Sponsors

Nanjing First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age 40-75 years old 2. ASA Grading II-III, NYHAI.-III, EF>=50% 3. Cardiac surgery under cardiopulmonary bypass (CPB) is planned

Exclusion criteria

Exclusion criteria: 1. Patients undergoing secondary cardiac surgery 2. Patients with intellectual disability, deafness, or mute or other conditions that affect normal communication 3. Previous neurological disease or psychiatric disease 4. History of sleep disorders requiring medical intervention (such as the use of sleeping pills) or PSOI score >=8 in the past month 5. Patients who are alcoholic, drug-addicted, and taking psychotropic drugs 6. Patients with obvious abnormal liver and kidney function affecting drug metabolism 7. Contraindications to the use of dexmedetomidine or esketamine

Design outcomes

Primary

MeasureTime frame
Post-operative sleep;

Countries

China

Contacts

Public ContactShi Hongwei

Department of Anesthesiology, Nanjing First Hospital, Nanjing Medical University

mdshw@163.com+86 189 5167 0892

Outcome results

None listed

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