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Sufentanil Intranasal

2019-10-28 13:56:49 | BioPortfolio

Summary

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

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 protocole level 1 and 3, the patients in the intervention arm are given classical level 1 medication as well as intranasal Sufentanil.

EVA level is then measured at 15-20 minutes and at 60 minutes. At both these time points, adverse effects and vitals are also assessed.

Study Design

Conditions

Emergencies

Intervention

Sufentanil

Status

Not yet recruiting

Source

Centre Hospitalier Universitaire Saint Pierre

Results (where available)

View Results

Links

Published on BioPortfolio: 2019-10-28T13:56:49-0400

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