Morphine
Conditions
Brief summary
The effect of epidural low-dose morphine-soaked microfibrillar collagen sponge in postoperative pain control after posterior lumbar spinal surgery: a randomized, double-blind, placebo-controlled study
Interventions
During posterior lumbar spinal surgery , patients received 1 mg morphine-soaked in epidural oxidized cellulose.
During posterior lumbar spinal surgery , patients received NSS -soaked in epidural oxidized cellulose.
Sponsors
Study design
Eligibility
Inclusion criteria
* Age \> 18 Yrs * Good orientation and communication
Exclusion criteria
* opioids or sulfonamides allergy * Contraindication for use * Epidural morphine * Selective COX 2 inhibitor * Patient-controlled analgesia (PCA) * ASA class \> 3 * BMI ≥ 35 kg/sq.m. * Preoperative use of opioids within 6 Wks * Intraoperative bleeding \> 1000ml
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS measurement was recorded at twenty-four hour after posterior lumbar spinal surgery then compare VAS between low-dose 1 mg morphine-soaked microfibrillar collagen sponge method with normal saline soked | 2 years |
Countries
Thailand