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Impairing Drugs and Alcohol as Risk Factors for Traumatic Injuries

Impairing Drugs and Alcohol as Risk Factors for Traumatic Injuries - a National Study on Injury Prevention

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03773614
Acronym
IDART
Enrollment
5000
Registered
2018-12-12
Start date
2019-03-01
Completion date
2020-02-29
Last updated
2021-06-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Trauma Injury

Brief summary

Impairing drugs and alcohol are major risk factors for traumatic injuries. Still there is to date little knowledge to what extent these factors affect the epidemiology of trauma. Detailed mapping of risk factors improve targeting and efficiency of primary injury prevention. The aim of this project is therefore to facilitate injury prevention through improved data collection and analysis on impairing drugs and alcohol as a contributing and modifiable factor in injury morbidity and mortality. Study question: What is the toxicological profile among patients with suspected severe traumatic injury? Study design: a prospective population-based and national observational study will analyse toxicology from blood samples of all trauma admission during a 12 month study period.

Interventions

None listed

Sponsors

University of Oslo
CollaboratorOTHER
Norwegian National Trauma Registry
CollaboratorUNKNOWN
Norwegian National Advisory Unit on Trauma
CollaboratorUNKNOWN
Norwegian Public Roads Administration
CollaboratorUNKNOWN
Norwegian Directorate of Health
CollaboratorOTHER_GOV
Norwegian Ministry of Transport and Communications
CollaboratorUNKNOWN
Sykehuset Innlandet HF
CollaboratorOTHER
Oslo University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* admission to any Norwegian Trauma Hospital (n=37) AND trauma team activation, during study period

Exclusion criteria

* age * foreign citizens

Design outcomes

Primary

MeasureTime frameDescription
Presence of alcohol in blood samples.Blood sample are collected at time of hospital admission for each participant. There is only one sample taken from each participant. Samples are consecutively analyzed during the study period. The database is analyzed after study period is completed.Alcohol is reported in grams per liter. Analysis of alcohol is performed with an automated enzymatic method using alcohol dehydrogenase.
Presence of impairing illicit and medicinal drugs in blood samples.Blood sample are collected at time of hospital admission for each participant. There is only one sample taken from each participant. Samples are consecutively analyzed during the study period.Impairing substances are reported as nanogram per milliliter. Analysis is performed using liquid chromatography coupled with mass spectrometry.

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026