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Clinical randomized controlled trial of multimodal analgesia (MMA) and patient controlled analgesia (PCA) in Oblique Lumbar Interbody Fusion

Clinical randomized controlled trial of multimodal analgesia (MMA) and patient controlled analgesia (PCA) in Oblique Lumbar Interbody Fusion

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042109
Enrollment
Unknown
Registered
2021-01-14
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-04-12

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

Conditions

Lumbar degenerative disease

Interventions

Multimodal Analgesia Experimental Group:1 hour before induction of anesthesia, oral celecoxib capsules 200 mg, pregabalin capsules 150 mg
Before the end of the operation, use ropivacaine injection 20ml: 150mg for local infiltration anesthesia at the operating area or screw entry site
After the patient was awake from anesthesia, he was intravenously infus
Patient controlled analgesia control group:After the patient is awake from anesthesia, a patient-controlled analgesia pump is placed intravenously, prepared with 100ug sufentanil citrate, 10mg tropise

Sponsors

Xinjiang Uygur Autonomous Region Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) The diagnosis of lumbar degenerative disease is clear, which seriously affects work and life. After strict conservative treatment, it is ineffective for 3-6 months. Surgical treatment is required, and there is no obvious surgical contraindication; (2) Symptoms, signs and imaging studies of lumbar degenerative disease are consistent; (3) The range of responsible lesions for lumbar degeneration is L2-L5; (4) The age of the patient is greater than 18 years; (5) The patient agrees to undergo oblique lateral lumbar interbody fusion and signs the surgical consent form.

Exclusion criteria

Exclusion criteria: (1) Degree III and IV lumbar spondylolisthesis; (2) Developmental spinal stenosis; (3) Severe osteoporosis; (4) Moderate to severe spinal deformity; (5) Obvious deformity of the extreme lateral side of the left iliac vein, which hinders the operation of the oblique lateral area of the L4/5 intervertebral disc; (6) A history of previous abdominal surgery, large scar formation in the left retroperitoneum area; (7) Infectious diseases such as spinal tuberculosis; (8) Those who have other serious liver, kidney, cardiovascular, blood system diseases, etc., are not recommended to use non-steroidal drugs after consultation with relevant departments; (9) Patients with active gastroduodenal ulcer; (10) Celecoxib should not be used for those allergic to sulfa drugs; (11) Patients who have been using analgesics for a long time before the operation and the time of withdrawal is less than 3 days; (12) Pregnant or lactating patients.

Design outcomes

Primary

MeasureTime frame
Early postoperative pain score;

Secondary

MeasureTime frame
The total number of PCA compressions, the total amount of drugs used in PCA, and additional remedial analgesia;Analgesia costs and length of hospital stay;

Countries

China

Contacts

Public ContactWei Hu

Second Department of Spine, Xinjiang Uygur Autonomous Region Hospital of Traditional Chinese Medicine

realhuwei@163.com+86 18199848111

Outcome results

None listed

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