lumbar surgery
Conditions
Interventions
Group 2:Modified-thoracolumbar interfascial plane block
Sponsors
The Second Affiliated Hospital of Anhui Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. For patients undergoing elective lumbar decompression and fusion surgery, the operation duration was >= 2 h; 2. Age 18-65 years, gender unlimited; 3. ASA grade I-III; 4. After fully explaining the content of the clinical trial, participants should voluntarily join and sign the informed consent.
Exclusion criteria
Exclusion criteria: 1. Patients with a history of scoliosis or spinal deformity, ankylosing spondylitis or suspected spinal cord injury; 2. There is coagulation dysfunction or an infected person at the puncture site; 3. Patients with previous allergies to local anesthetics or non-steroidal drugs; 4. Patients with chronic pain and long-term oral painkillers; 5. Complicated with serious diseases, such as abnormal liver and kidney function, abnormal lung function, arrhythmia or cardiac insufficiency; 6. Poor control of diabetes and hypertension; 7. Patients judged to lack the ability to consent; 8. Patients deemed unsuitable for study participation by other clinical responsible physicians or clinical responsible physicians.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 15-item Quality of Recovery (QoR-15) scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative pain score;Postoperative opioid dosage;Postoperative patient satisfaction score; | — |
Countries
China
Contacts
Public ContactYun Li
The Second Affiliated Hospital of Anhui Medical University
Outcome results
None listed