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A prospective study of different postoperative analgesic regimens on the rehabilitation quality of elderly patients undergoing thoracolumbar spine surgery

A prospective study of different postoperative analgesic regimens on the rehabilitation quality of elderly patients undergoing thoracolumbar spine surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102525
Enrollment
Unknown
Registered
2025-05-15
Start date
2023-05-08
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Postoperative pain after lumbar spine surgery

Interventions

Control Group:Fentanyl 15 µg/kg + tropisetron 10 mg + normal saline was configured into a 300 ml patient-controlled analgesic pump. Intravenous fentanyl 2 µg/kg was injected 30 minutes before the oper
Fentanyl plus acetaminophen group:Fentanyl 10 µg/kg + acetaminophen 2 g + tropisetron 10 mg + normal saline were configured into a 300 ml patient-controlled analgesic pump. Acetaminophen 500mg was int
Fentanyl plus acetaminophen and flurbiprofen ester group:Fentanyl 10 µg/kg + acetaminophen 2 g + flurbiprofen cilexil 200 mg + tropisetron 10 mg + normal saline were configured into a 300 ml patient-c

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=65 years old, ASA grade I-III 2. Thoracolumbar interbody fusion 3. Surgery under general anesthesia 4. Can sign informed consent and have the ability to read and write.

Exclusion criteria

Exclusion criteria: 1. Refuse to participate in this experiment. 2. Emergency surgery. 3. Patients with incomplete data. 4. Those with severe dementia, speech impairment, hearing or visual impairment who are unable to complete the questionnaire. 5. Patients with severe cardiopulmonary, liver and kidney dysfunction before surgery. 6. Those with a history of chronic pain and long-term use of analgesic and sedative drugs. 7. Patients with mental illness and cognitive dysfunction.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale,VAS;Pain;EQ-5D;PCS score;Mini Cog score;Indicators of liver function;Indicators of renal function;

Secondary

MeasureTime frame
Patient's anesthesia duration during surgery;Sex;Age;Body mass index; Analgesic pump usage;Blood count;

Countries

China

Contacts

Public ContactWeixin Dai

The First Affiliated Hospital of Guangxi Medical University

180daiweixin@163.com+86 135 0771 3016

Outcome results

None listed

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