Status:
COMPLETED
IV Paracetamol, Dexketoprofen or Morphine for the Treatment of Low Back Pain
Lead Sponsor:
Pamukkale University
Conditions:
Low Back Pain
Eligibility:
All Genders
16-55 years
Phase:
PHASE4
Brief Summary
This randomized, controlled trial evaluates the analgesic efficacy and safety of intravenous single-dose paracetamol, dexketoprofen and morphine for the treatment of low back pain.
Detailed Description
Study Design and Setting: This is a single-center, prospective, randomized, double-blind, clinical trial performed in an ED of a tertiary care hospital with annual census of approximately 37.000 visi...
Eligibility Criteria
Inclusion
- Adults (aged 16 to 55 years) with acute low back pain were eligible for inclusion in the study- -
Exclusion
- Exclusion criteria included known allergy or contraindication to morphine, paracetamol,dexketoprofen or any opioid analgesic
- Hemodynamic instability
- Fever (temperature \>38°C \[100.4°F\])
- Evidence of peritoneal inflammation
- Documented or suspected pregnancy
- Known or suspected aortic dissection or aneurysm, lombar disc hernia
- Use of any analgesic within 6 hours of ED presentation
- Previous study enrollment.
- Patients with known renal, pulmonary, cardiac, or hepatic failure, as well as those with renal transplantation, were also excluded.
Key Trial Info
Start Date :
January 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2011
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT01422291
Start Date
January 1 2011
End Date
July 1 2011
Last Update
August 23 2011
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