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Effect of Total Intravenous Anesthesia with Ciprofol on Early Recovery Quality in Elderly Patients Undergoing Posterior Lumbar Interbody Fusion

Effect of Total Intravenous Anesthesia with Ciprofol on Early Recovery Quality in Elderly Patients Undergoing Posterior Lumbar Interbody Fusion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107715
Enrollment
Unknown
Registered
2025-08-18
Start date
2025-09-08
Completion date
Unknown
Last updated
2025-08-25

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

Conditions

Lumbar spinal stenosis, lumbar disc herniation

Interventions

Propofol group (group P):(1) Induction of anesthesia: in group P, anesthesia was induced with propofol 1.5 mg/kg, sufentanil 0.3µg/kg and rocuronium 0.6 mg/kg. (2) Anesthesia maintenance: In group P,
(C):(1) Induction of anesthesia: in group C, anesthesia was induced with ciprofol 1.5 mg/kg, sufentanil 0.3µg/kg and rocuronium 0.6 mg/kg. (2) Anesthesia maintenance: In group C, ciprofol 2.5-7.5 mg·k

Sponsors

Xuanwu Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Men and women are not limited; 2. Age 65-85 years old; 3. 18 kg/m2 < BMI < 28 kg/m2; 4. American Society of Anesthesiologists (ASA) grade I-III; 5. Patients undergoing posterior lumbar fusion under general anesthesia with endotracheal intubation; 6. Consent to participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. History of cardiovascular disease including severe hypertension (systolic blood pressure >=180 mmHg), unstable angina pectoris, severe arrhythmia, and cardiac insufficiency; 2. Patients were complicated with endocrine diseases and severe liver and renal dysfunction before operation; 3. Respiratory failure (PaO2<60mmHg); 4. The history of stroke was less than 3 months; 5. Patients were allergic to cyclopropofol, propofol and other drugs and their drug components; 6. Patients with a previous history of mental illness or dementia who were unable to cooperate with the completion of the study; 7. Patients who planned to undergo surgery for 4 or more spinal segments; 8. The patient and family members declined to participate in the study.

Design outcomes

Primary

MeasureTime frame
QoR-15 score;

Secondary

MeasureTime frame
QoR-15 score;The occurrence of intraoperative adverse events;The use of vasoactive drugs during operation;Intraoperative consumption of ciprofol;Intraoperative consumption of propofol;Intraoperative consumption of remifentanil ;Intraoperative consumption of sufentanil;Recovery time ;Extubation time;RASS score;Blood Glucose Level;The occurrence of postoperative complications;Postoperative HOSPITAL STAY;Postoperative first flatus time;Postoperative first defecation time;Postoperative NRS pain scores at rest and during activity (cough);

Countries

China

Contacts

Public ContactMa Yanhui

Xuanwu Hospital, Capital Medical University

peep2005@163.com+86 158 1093 0059

Outcome results

None listed

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