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A prospective RCT study of hemodynamics and postoperative recovery quality induced by sodium oxybutyrate combined with propofol in spinal surgery

A prospective RCT study of hemodynamics and postoperative recovery quality induced by sodium oxybutyrate combined with propofol in spinal surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080686
Enrollment
Unknown
Registered
2024-02-05
Start date
2024-02-20
Completion date
Unknown
Last updated
2024-02-11

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

Conditions

Spinal Surgery

Interventions

Group B:sodium oxybutyrate combined with propofol

Sponsors

Department of Anesthesiology, Tsinghua University Yuquan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 40-80 years old; 2. Spinal surgery is to be performed under general anesthesia, and the expected operation time is =2 hours; 3. A self-controlled intravenous analgesic pump is needed after surgery.

Exclusion criteria

Exclusion criteria: 1. Preoperative communication is not possible due to visual, auditory, language or other reasons; 2. Spinal orthopaedic surgery; 3. Patients with severe bradycardia (HR<50 beats/min), sick sinus syndrome, grade 2 or above atrioventricular block without pacemaker implantation; 4. Severe liver function impairment (Child-Pugh grade C); 5. Renal failure (requiring kidney replacement therapy); 6. Participate in other clinical studies.

Design outcomes

Primary

MeasureTime frame
hemodynamics;Postoperative pain score;

Secondary

MeasureTime frame
Quantity of each drug used in perioperative period;Intraoperative adverse events;Postoperative delirium score;PCA dosage;Patient satisfaction score;Major post-operative laboratory results;

Countries

China

Contacts

Public ContactFan Ting

Department of Anesthesiology, Tsinghua University Yuquan Hospital

13681100715@163.com+86 136 8110 0715

Outcome results

None listed

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