Skip to content

The effect of remifentanil on emergence and sleep quality in elderly patients undergoing spinal surgery under general anesthesia

Effect of remimazolam on emergence and postoperative sleep quality after general anesthesia after spinal surgery in elderly patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110216
Enrollment
Unknown
Registered
2025-10-10
Start date
2025-10-25
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Delayed recovery after general anesthesia, postoperative delirium, cognitive impairment, postoperative sleep disorders, etc.

Interventions

Experimental group:A general anesthetic regimen with remimazolam as the main one is used
Control group:Use a total anesthesia scheme mainly based on propofol.

Sponsors

Hebei Medical University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Age 60~85 years old; 2. Preoperative PSQI < 7 points; 3. ASA Level I-III; 4. Body mass index BMI<=35kg/m^2; 5. Gender is not limited; 6. Patients undergoing downward spine surgery under general anesthesia; 7. Patients who are proposed to undergo experimental protocol A/B: A. The experimental group uses remimazolam, sufentanil, and cis-atracurium for induction anesthesia; Anesthesia is maintained with remimazolam and remifentanil. Sevoflurane is applied as necessary during induction and maintenance. B. The control group was given propofol, sufentanil, and cis-atracurium for induction anesthesia. Maintain anesthesia with propofol and remifentanil. Sevoflurane application if necessary during induction and maintenance;

Exclusion criteria

Exclusion criteria: 1.For individuals allergic to research drugs; 2.Recently abused sleep aid drugs; 3.Patients with communication barriers; 4.Severe liver and kidney dysfunction; 5.Merge other injuries that require simultaneous surgery; 6.Emergency operation; 7.Patients transferred to ICU after surgery; 8.Patients who did not use pain pumps after surgery;

Design outcomes

Primary

MeasureTime frame
Quality of awakening;

Secondary

MeasureTime frame
Demographic information;Sleep quality;Adverse event;Anesthesia surgery information;

Countries

China

Contacts

Public ContactZhao Shuang

Hebei Medical University Third Hospital

zhaoshuang810924@163.com+86 311 8860 3000

Outcome results

None listed

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