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Sublingual Versus Endovenous Fentanyl for Pain Treatment in Trauma Patients in the Emergency Room

NCT03080324 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 108

Last updated 2020-03-04

No results posted yet for this study

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.

Conditions

  • Acute Pain Due to Trauma

Interventions

DRUG

Fentanyl sublingual

Fentanyl sublingual

DRUG

Fentanyl ev

Fentanyl ev

DRUG

Placebo sublingual

Placebo sublingual

DRUG

Placebo ev

Saline

Sponsors & Collaborators

  • Azienda Sanitaria dell'Alto Adige

    lead OTHER

Principal Investigators

  • Elisabeth Gruber, MG MSc · Südtiroeler Sanitätsbetrieb

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-12-01
Primary Completion
2017-05-15
Completion
2017-05-15

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03080324 on ClinicalTrials.gov