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Is There an Ideal Dose of Intravenous Fentanyl in the Prehospital Setting

Primary Purpose

Acute Pain

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Fentanyl
Sponsored by
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Pain focused on measuring Emergency Medical Services, Analgesics

Eligibility Criteria

undefined - 110 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with acute pain treated with intravenous fentanyl by ambulance personnel

Exclusion Criteria:

  • Reduced conscious level (GCS < 15) before initiation of fentanyl treatment
  • Reduced respiratory rate (< 10/minute) before initiation of fentanyl treatment
  • Patient weight < 30 kg
  • Known opioid allergy
  • Women in labour
  • Chronic pain conditions

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    No Intervention

    Experimental

    Arm Label

    Existing treatment

    More liberal treatment

    Arm Description

    Business as usual: Ambulance personnel use existing treatment approach (a total of 2 μg/kg fentanyl per transport)

    Ambulance personnel use a more liberal treatment approach (a total of 3 μg/kg fentanyl per transport)

    Outcomes

    Primary Outcome Measures

    Proportion of patients with sufficient pain relief (NRS < 4) at hospital arrival

    Secondary Outcome Measures

    Proportion of patients with reduced Glasgow Coma Scale (<15) after fentanyl administration and at any given point during transport
    Proportion of patients with reduced respiratory rate (<10/minute) after fentanyl administration and at any given point during transport
    Proportion of patients with reduced peripheral oxygen saturation (< 90%) after fentanyl administration and at any given point during transport
    Proportion of patients with hypotension after fentanyl administration and at any given point during transport
    Hypotension defined as a drop in mean arterial pressure (MAP) >= 10 mmHg to a MAP < 70 mmHg

    Full Information

    First Posted
    September 12, 2016
    Last Updated
    October 25, 2017
    Sponsor
    University of Aarhus
    Collaborators
    Central Denmark Region
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02914678
    Brief Title
    Is There an Ideal Dose of Intravenous Fentanyl in the Prehospital Setting
    Official Title
    Is There an Ideal Dose of Intravenous Fentanyl in the Prehospital Setting: A Prospective Cluster-randomized Comparison of 2 vs. 3 μg/kg/Transport
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2017
    Overall Recruitment Status
    Completed
    Study Start Date
    October 2016 (Actual)
    Primary Completion Date
    October 2017 (Actual)
    Study Completion Date
    October 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University of Aarhus
    Collaborators
    Central Denmark Region

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    In a previous study the investigators evaluated the apparent efficacy and safety of intravenous fentanyl administered by ambulance personnel and found that 58.4% (CI 56.4-60.4) out of 2348 prehospital patients treated with fentanyl still experienced moderate to severe pain [numeric rating scale (NRS, 0-10) > 3] at hospital arrival. The number of patients with possible fentanyl-related side effects was low. Therefore, the aim of the present study is to explore the efficacy and safety of a liberalized pain treatment protocol for ambulance personnel (a total of 3 μg/kg per transport) compared with existing restrictive protocol (a total of 2 μg/kg per transport). The investigators hypothesize that: A higher proportion of patients will experience sufficient pain relief at hospital admission (NRS < 4) using the liberalized protocol and There will be no differences in the proportion of potential fentanyl related side-effects are observed.
    Detailed Description
    A prospective cluster-randomized trial observing proportional differences in sufficient pain relief at hospital admission (NRS < 4) and potential fentanyl related side-effects between patients treated by ambulance personnel applying either: a more liberal treatment approach (a total of 3 μg/kg per transport) or existing treatment approach (a total of 2 μg/kg per transport). The Ambulance stations and their affiliated ambulance personnel are stratified into 5 clusters according to size/average transports per month and randomized to either liberal or existing treatment approach within each cluster. As patients are not randomized on an individual level baseline differences between the two groups and its patients are adjusted statistically with relevant confounders on 3 overall levels: Patients: Charlson Comorbidity Index Score, main overall diagnose category, inhospital surrogate measures of disease severity (intensive care unit admission and 30-day mortality). Ambulance personnel: Years of experience and preinterventional cumulative fentanyl administration and Ambulance stations and geographical factors: prehospital time measures and geographical distance from site of emergency to hospital. These covariates are obtained from the Danish National Patient Registry, the Danish Civil Registration System and the electronic prehospital patient journal.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Acute Pain
    Keywords
    Emergency Medical Services, Analgesics

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    7093 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Existing treatment
    Arm Type
    No Intervention
    Arm Description
    Business as usual: Ambulance personnel use existing treatment approach (a total of 2 μg/kg fentanyl per transport)
    Arm Title
    More liberal treatment
    Arm Type
    Experimental
    Arm Description
    Ambulance personnel use a more liberal treatment approach (a total of 3 μg/kg fentanyl per transport)
    Intervention Type
    Other
    Intervention Name(s)
    Fentanyl
    Intervention Description
    Change in protocol from 2 to a total of 3 μg/kg fentanyl per transport
    Primary Outcome Measure Information:
    Title
    Proportion of patients with sufficient pain relief (NRS < 4) at hospital arrival
    Time Frame
    Up to 6 hours
    Secondary Outcome Measure Information:
    Title
    Proportion of patients with reduced Glasgow Coma Scale (<15) after fentanyl administration and at any given point during transport
    Time Frame
    Up to 6 hours
    Title
    Proportion of patients with reduced respiratory rate (<10/minute) after fentanyl administration and at any given point during transport
    Time Frame
    Up to 6 hours
    Title
    Proportion of patients with reduced peripheral oxygen saturation (< 90%) after fentanyl administration and at any given point during transport
    Time Frame
    Up to 6 hours
    Title
    Proportion of patients with hypotension after fentanyl administration and at any given point during transport
    Description
    Hypotension defined as a drop in mean arterial pressure (MAP) >= 10 mmHg to a MAP < 70 mmHg
    Time Frame
    Up to 6 hours

    10. Eligibility

    Sex
    All
    Maximum Age & Unit of Time
    110 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients with acute pain treated with intravenous fentanyl by ambulance personnel Exclusion Criteria: Reduced conscious level (GCS < 15) before initiation of fentanyl treatment Reduced respiratory rate (< 10/minute) before initiation of fentanyl treatment Patient weight < 30 kg Known opioid allergy Women in labour Chronic pain conditions
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Kristian Friesgaard, MD, PhD Student
    Organizational Affiliation
    University of Aarhus
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Lone Nikolajsen, DmSc
    Organizational Affiliation
    Aarhus University Hospital
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Hans Kirkegaard, Professor
    Organizational Affiliation
    Aarhus University Hospital
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Erika Frischknecht Christensen, Professor
    Organizational Affiliation
    Northern Denmark Region
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Matthias Giebner, MD
    Organizational Affiliation
    Central Denmark Region
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Claus-Henrik Rasmussen, MD
    Organizational Affiliation
    Central Denmark Region
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    26612100
    Citation
    Friesgaard KD, Nikolajsen L, Giebner M, Rasmussen CH, Riddervold IS, Kirkegaard H, Christensen EF. Efficacy and safety of intravenous fentanyl administered by ambulance personnel. Acta Anaesthesiol Scand. 2016 Apr;60(4):537-43. doi: 10.1111/aas.12662. Epub 2015 Nov 27.
    Results Reference
    background
    PubMed Identifier
    21775347
    Citation
    Lynge E, Sandegaard JL, Rebolj M. The Danish National Patient Register. Scand J Public Health. 2011 Jul;39(7 Suppl):30-3. doi: 10.1177/1403494811401482.
    Results Reference
    background
    PubMed Identifier
    24965263
    Citation
    Schmidt M, Pedersen L, Sorensen HT. The Danish Civil Registration System as a tool in epidemiology. Eur J Epidemiol. 2014 Aug;29(8):541-9. doi: 10.1007/s10654-014-9930-3. Epub 2014 Jun 26.
    Results Reference
    background
    PubMed Identifier
    30732618
    Citation
    Friesgaard KD, Kirkegaard H, Rasmussen CH, Giebner M, Christensen EF, Nikolajsen L. Prehospital intravenous fentanyl administered by ambulance personnel: a cluster-randomised comparison of two treatment protocols. Scand J Trauma Resusc Emerg Med. 2019 Feb 7;27(1):11. doi: 10.1186/s13049-019-0588-4.
    Results Reference
    derived

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    Is There an Ideal Dose of Intravenous Fentanyl in the Prehospital Setting

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