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NCT02836509Phase 4
Key facts
Phase 4, randomised, double-blind trial in low back pain (LBP) comparing Paracetamol Group with Ibuprofen Group (2 arms). Primary endpoint: Reduction of Low Back Pain on the Visual Analog Scale. Status: unknown.
Paracetamol Group
1000 mg Paracetamol in 150 ml normal saline IV.
Ibuprofen Group
800 mg Ibuprofen in 150 ml normal saline IV.
Adult patients (21-80 years) presenting to the ED with low back pain starting in the last week. Excludes patients with chronic pain, neurological symptoms, hypotension, fever, peptic ulcer, or recent analgesic use.
Reduction of Low Back Pain on the Visual Analog Scale
Adverse events
Beyond the preview
Full results, competitive context and analysis are in the Gosset platform.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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