MedPath

Perioperative Duloxetine and Etoricoxib improve postoperative pai

Not Applicable
Completed
Conditions
Surgery
Postoperative pain after laminectomy surguries
Registration Number
ISRCTN48329522
Lead Sponsor
Al-Minia University
Brief Summary

2017 results in https://pubmed.ncbi.nlm.nih.gov/29197345/ (added 26/11/2020)

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
120
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

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

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
<br> 1. The time to first rescue analgesic is routinely 24h and 48h postoperatively<br> 2. Total morphine consumption is measured by calculating the doses at 24 and 48 hours post-operatively<br> 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<br> 4. Patient satisfaction is measured using a numerical rating scale (NRS) at 24 hours post-operatively<br>
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