Clinical Trials Directory

Trials / Completed

CompletedNCT01564680

Lornoxicam vs. Paracetamol After Lower Abdominal Surgery

Intravenous Lornoxicam is More Effective Than Paracetamol as a Supplemental Analgesic After Lower Abdominal Surgery; A Randomized Controlled Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Imam Abdulrahman Bin Faisal University · Academic / Other
Sex
All
Age
18 Years – 69 Years
Healthy volunteers
Not accepted

Summary

Background: The aim of this prospective, randomized, double-blind study is to determine the most effective supplemental analgesic, paracetamol or lornoxicam for postoperative pain relief after lower abdominal surgery. Methods: Sixty patients scheduled for lower abdominal surgery under general anesthesia were randomly allocated to receive either isotonic saline (Control group), intravenous paracetamol 1 g every 6 h (Paracetamol group) or lornoxicam 16 mg then 8 mg after 12 h (Lornoxicam group). Additionally pain was treated postoperatively using morphine patient-controlled analgesia. Postoperative pain scores measured by the verbal pain score (VPS), morphine consumption and the incidence of side effects were measured at 1, 2, 4, 8, 12 and 24 hours postoperatively.

Conditions

Interventions

TypeNameDescription
OTHERplacebonormal saline
DRUGParacetamolIV paracetamol infusion
DRUGLornoxicam16 mg at skin closure and 8 mg 12 hours postoperative

Timeline

Start date
2009-03-01
Primary completion
2011-03-01
Completion
2011-03-01
First posted
2012-03-28
Last updated
2012-03-28

Locations

1 site across 1 country: Saudi Arabia

Source: ClinicalTrials.gov record NCT01564680. Inclusion in this directory is not an endorsement.