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Clinical Trial Summary

Study of the effects of intranasal sufentanil on patients presenting to the emergency department with acute post-traumatic pain.


Clinical Trial Description

In this study, patients presenting to the emergency department with post-traumatic pain of 7 or more on the visual analog pain scale, since less than 24 hours, in the limbs, spine or thorax are randomized in a control arm or an interventional arm. The patients in the control arm will receive the institution's classical analgetic protocol level 1 and 3, the patients in the intervention arm are given classical level 1 medication as well as intranasal Sufentanil. Pain is then measured using the Visual Analogue Pail Scale at 15-20 minutes and at 60 minutes. At both these time points, adverse effects and vitals are also assessed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04137198
Study type Interventional
Source Centre Hospitalier Universitaire Saint Pierre
Contact Bernard Kreps, MD
Phone +3225353495
Email bernard_kreps@stpierre-bru.be
Status Recruiting
Phase Phase 4
Start date January 22, 2020
Completion date September 1, 2025

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