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Clinical Trial Summary

The purpose of this study is to determine the non-inferiority of the efficacy of sublingual given fentanyl versus endovenous given fentanyl for patients in the emergency departement.


Clinical Trial Description

Fentanyl endovenous (ev) is an excellent analgesic drug for pain relief in acute traumatic pain. Fentanyl sublingual (Abstral ®) is an excellent analgesic drug in the breakthrough pain relief in oncologic patients.

The immediate (10 minutes) effect and the ease of administration of sublingual fentanyl could be a possibility for a fast pain relief in remote areas such as mountain rescue missions.

Patients will be recruited according to a randomized list to fentanyl ev or fentanyl sublingual versus placebo oral or placebo ev.

Safety issues like control of vital signs will be warranted ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03080324
Study type Interventional
Source Azienda Sanitaria dell'Alto Adige
Contact
Status Completed
Phase Phase 4
Start date December 1, 2016
Completion date May 15, 2017

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