SPINALFUSION and postoperative pain M43.1
Conditions
Interventions
Group 1: Levobupivacaine via epidural catheter: after the epidural catheter insertion the patients got 0,125% levobupivacaine in the dosage after Bromage and then 0,125% lev0bupivacaine 0,1ml/kg /h fo
Sponsors
UKC Ljubljana
Eligibility
Sex/Gender
All
Age
30 Years to 80 Years
Inclusion criteria
Inclusion criteria: patients between 30-80 years ASA 1-3 spondylolystesis with spinal fusion and instrumentation
Exclusion criteria
Exclusion criteria: mental illness drug addiction renal or hepatic insufficiency spondylodiscitis neurological deficits known allergy to local anesthetics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS (visuel analog scale) pain score each 6hours for 5 days, analgesics consuption in summary for 5 days, cortisol, blood glucose and cholesterol level before surgery and for 4 postoperative days each day, days day of hospital stay | — |
Secondary
| Measure | Time frame |
|---|---|
| peristalsis after 24 hours, side effects, postoperative bleeding, time to first postoperative defecation | — |
Countries
Slovenia
Contacts
Public ContactDarja Servicl Kuchler
UKC Ljubljana
Outcome results
None listed