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Timecost of Intranasal Versus Intravenous Analgesia in Traumatic Pain

A

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Status

Completed

Conditions

Acute Pain Due to Trauma
Analgesia

Treatments

Other: Intranasal administration
Other: Intravenous administration

Study type

Interventional

Funder types

Other

Identifiers

NCT06351137
INIV2023

Details and patient eligibility

About

Prehospital treatment of acute traumatic pain is common in military practice. Analgesics are usually administered intravenously (IV). Research from the civil prehospital environment shows that obtaining IV access can be difficult and time consuming, delaying onset of treatment. The challenges for obtaining IV access in the military prehospital setting are even bigger, for example in combat environments. However, this has not been assessed.

Current guidelines also offer alternative routes of administration for analgesics, for example intranasal (IN) administration. IN administration is a fast, easy and effective route of administration. This study determines whether IN administration of analgesia is faster and leads to increased healthcare provider satisfaction compared to IV administration in patients with acute traumatic pain in a simulated military prehospital environment.

Enrollment

19 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • All navy healthcare personnel attending (simulation) training on prehospital trauma care.

Exclusion Criteria: none

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

19 participants in 2 patient groups

IV first
Other group
Description:
Subjects in this group will be instructed to use intravenous administration in the first scenario and use intranasal administration in the second scenario.
Treatment:
Other: Intravenous administration
Other: Intranasal administration
IN first
Other group
Description:
Subjects in this group will be instructed to use intranasal administration in the first scenario and use intravenous administration in the second scenario.
Treatment:
Other: Intravenous administration
Other: Intranasal administration

Trial contacts and locations

1

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Central trial contact

Midas N de Grunt, MD; Robert P Weenink, PhD

Data sourced from clinicaltrials.gov

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