Impairing Drugs and Alcohol as Risk Factors for Traumatic Injuries
NCT ID: NCT03773614
Last Updated: 2021-06-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
5000 participants
OBSERVATIONAL
2019-03-01
2020-02-29
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Secondary Prevention and Recidivism Reduction in Trauma Patients
NCT03967262
Recovery - a Collaborative Project
NCT04138459
Aerobic Exercise for Cognitive Functioning in Patients With Substance Use Disorder
NCT05324085
Factors Predicting Outcome in Group Treatment of Alcohol Use Disorders (AUDs)
NCT04822987
Multidisciplinary Approach to Reduce Injury and Substance Abuse
NCT01048359
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* foreign citizens
16 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Oslo
OTHER
Norwegian National Trauma Registry
UNKNOWN
Norwegian National Advisory Unit on Trauma
UNKNOWN
Norwegian Public Roads Administration
UNKNOWN
Norwegian Directorate of Health
OTHER_GOV
Norwegian Ministry of Transport and Communications
UNKNOWN
Sykehuset Innlandet HF
OTHER
Oslo University Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Thomas Kristiansen
Principal Investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
OsloUH
Oslo, , Norway
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2017/1363
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.