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Clinical Trial Summary

The aim of the study is to evaluate the efficacy and safety of different dosage regimens of the combination methocarbamol/paracetamol in the treatment of patients with acute non-specific Low Back Pain.


Clinical Trial Description

This is a Phase IV, randomized, open-label, parallel-group, multicentre study. A total of 192 patients of both sexes will be enrolled in the study and will be randomized 1:1 to one of the following 2 treatment groups: - Group 1: methocarbamol 380 mg/paracetamol 300 mg (2 oral tablets 4 times/day) - Group 2: methocarbamol 380 mg/paracetamol 300 mg (2 oral tablets 6 times/day) The expected duration of patient participation into the trial (from ICF signature up to any applicable follow up) is 8 days (± 1). Patients enrolment will be competitive among clinical sites. The primary endpoint will be the Time to complete relief of pain, defined as the time when the complete pain relief is reached. A Complete pain relief is defined as a VAS score ≤ 5 mm at two consecutive assessments starting from Day1 up to Day7 (±1). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05204667
Study type Interventional
Source Aziende Chimiche Riunite Angelini Francesco S.p.A
Contact
Status Suspended
Phase Phase 4
Start date October 7, 2021
Completion date April 30, 2024

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