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Epidemiology of Acute Self-poisoning in Emergency Services in France

Evaluation of the Epidemiology and the Take Load of Voluntary Drug Intoxications by the Emergency Structures in France

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02518386
Acronym
EpiTox
Enrollment
700
Registered
2015-08-07
Start date
2015-03-31
Completion date
2016-06-30
Last updated
2019-04-17

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

Conditions

Suicide Attempts

Keywords

emergency department, epidemiology, prehospital care, dispatch, acute self poisoning

Brief summary

Acute self poisoning is a leading cause of suicide attempts and leads to frequent emergency department visits. However, the exact epidemiology of acute self poisoning is not known. The description of the clinical pathway and the characteristics of patients with acute self poisoning could lead to an improvement in emergency care. The Investigators will conduct a 48h observational study in emergency services in France. Investigators primary objective is to gathered epidemiological clinical and treatment data during emergency dispatch, prehospital care and inhospital emergency care.

Detailed description

Acute self poisoned patients will be prospectively and anonymously recruited by emergency physicians in charge during two days. Acute self poisoning is define as follow: intentional medicine intake in the 24h hours before emergency department admission. Epidemiological, clinical, toxicological and treatment data will be gathered. Outcome of patient will be prospectively assessed at 30days. All data will be transmitted to the principal investigators. Then, 20% of the data will be monitored by an independent committee. Exhaustivity will be retrospectively assessed by the number of inclusions in 10 emergency centers divided by the total number of possible inclusions in these centers. Finally, an independent statistician will be in charge of the analysis.

Interventions

OTHERNo intervention

No intervention is planned

Sponsors

French Society of Emergency Medicine
CollaboratorOTHER
University Hospital, Grenoble
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* acute self poisoning defined as the intentional intake (oral, nasal, injection etc.) of medicines during the 24h before first medical contact

Exclusion criteria

* cardiac arrest at first medical contact (dispatch or physician) * acute self poisoning without any medication intake * non intentional poisoning

Design outcomes

Primary

MeasureTime frame
Percentage of each drug class48h

Secondary

MeasureTime frameDescription
Mortality according to drug class ingestion30 days
ICU admission according to drug class ingestion30 days
icu admission (percentage)48h
percentage of errors according to the Grenoble clinical decision rule30 days
multivariate analysis to describe factors associated with ICU admission30 days
multivariate analysis to describe factors associated with mobile intensive care unit dispatch30 days
odds ratio of drug classes according to sexe and age48h
Time (median) of admission according unit of admission48h
prehospital and inhospital mortality30 days
percentage of each antidotal treatment48h
mobile intensive care unit (percentage) dispatch30 days
Age according to drug classes ingestion48hMedian age compared according drug classes ingestion
Gender according to drug classes ingestion48hPourcentage of gender compared according drug classes ingestion
Time (median) of admission according to drug classes ingestion48h
number of participants with poisoning incident48h

Outcome results

None listed

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