Actively Recruiting

Age: 1Year - 17Years
All Genders
NCT06832046

Evaluation of the "Intranasal Fentanyl" Protocol in Pediatric Surgical Emergencies at Strasbourg University Hospital

Led by University Hospital, Strasbourg, France · Updated on 2025-02-18

500

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Emergency trauma departments receive thousands of patients each year whose main symptom is pain. In recent years, intranasal fentanyl (FIN) has entered the therapeutic arsenal to treat pain in the emergency department. Various studies have validated its effectiveness for musculoskeletal pain as well as its tolerance and safety of use. Since then, new protocols have been implemented including this treatment. In This study, the investigators propose to retrospectively study the quality of prescription of intranasal fentanyl in the treatment of pain in the emergency department and the quality of monitoring of this treatment in current practice.

CONDITIONS

Official Title

Evaluation of the "Intranasal Fentanyl" Protocol in Pediatric Surgical Emergencies at Strasbourg University Hospital

Who Can Participate

Age: 1Year - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Child under 18 years old
  • Child treated in the pediatric emergency department of Strasbourg University Hospital
  • Child who received intranasal fentanyl between 08/01/2022 and 09/31/2024
  • Child and/or parent or guardian has not objected to reuse of health data for this research
Not Eligible

You will not qualify if you...

  • Child or parent/guardian refuses to participate in the study
  • Patient's medical file is incomplete
  • Child is not living in France

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Service d'Urgences Médico-Chirurgicales Pédiatriques - CHU de Strasbourg - France

Strasbourg, France, 67091

Actively Recruiting

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Research Team

D

Dimitar TCHOMAKOV, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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