Postoperative pain after laminectomy surguries Surgery Postoperative pain after laminectomy surguries
Conditions
Interventions
Patients admitted to the hospital are randomised using computer-generated random numbers with closed-sealed envelopes into one of the four groups of 30 patients.
Group 1: Participants
Sponsors
Al-Minia University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patients with an ASA physical status of I, II and III scheduled for single level lumbar spinal disc prolapsed surgery 2. Can provide written informed consent 3. Aged between 18 and older
Exclusion criteria
Exclusion criteria: 1. History of allergic reaction to any of the study drugs 2. History of drug or alcohol abuse 3. Abnormal renal or liver function tests. 4. Patients using antidepressants who did not stop taking them two weeks before surgery 5. Patients with previous cervical surgeries, psychiatric disorders and patients receiving opioid analgesic medications within 24 hours preoperatively
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain is measured using pain assessment measures and questions 30 minutes after the end of anesthesia and two, four, six, 12, 24 and 48 hours post-operatively | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. The time to first rescue analgesic is routinely 24h and 48h postoperatively 2. Total morphine consumption is measured by calculating the doses at 24 and 48 hours post-operatively 3. Side effects, including headache, rash, nausea, vomiting, dizziness and drowsiness are recorded. The severity of postoperative nausea and vomiting (PONV) is graded on a four-point ordinal scale 4. Patient satisfaction is measured using a numerical rating scale (NRS) at 24 hours post-operatively | — |
Countries
Egypt
Outcome results
None listed