Sufentanil Intranasal

Status Recruiting

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

Clinical Trial Details

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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