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Clinical Trial Summary

The purpose of this study is to monitor severe pain for femur fracture after treatment with paracetamol IV or OR.


Clinical Trial Description

We enrolled 170 consecutive patients with femur fracture and severe pain. They received an initial analgesic treatment with paracetamol orally (OR) or intravenously (IV). The primary outcome was the reduction of pain of 1 point at visual analogue scale for pain (VAS) after the 1 st hour of treatment (T1). Secondary endpoints included the reduction of pain of at least 2 points on the VAS scale at the 4 th hour (T4), the need of rescue therapy and the number of adverse events. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05025228
Study type Observational
Source Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Contact
Status Completed
Phase
Start date June 1, 2019
Completion date June 30, 2020

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