An observational study in Suicide Attempts, sponsored by University Hospital, Grenoble. Completed. Per ClinicalTrials.gov, last updated 2019-04-17.
Sponsored by University Hospital, Grenoble · Observational
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.
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.
1,692 studies on the registry are indexed under Emergencies; 333 are open to participants now.
This study's enrollment of 700 is above the median of 353 across 714 observational studies indexed under Emergencies.
Browse Emergencies studies →University Hospital, Grenoble is the lead sponsor of 815 studies on the registry; 205 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Patients dispatched of admitted for acute self poisoning in emergency medical services and/or emergency departments
Exclusion Criteria:
No intervention is planned
Percentage of each drug class
Time frame: 48h
odds ratio of drug classes according to sexe and age
Time frame: 48h
number of participants with poisoning incident
Time frame: 48h
prehospital and inhospital mortality
Time frame: 30 days
percentage of each antidotal treatment
Time frame: 48h
mobile intensive care unit (percentage) dispatch
Time frame: 30 days
Age according to drug classes ingestion
Median age compared according drug classes ingestion
Time frame: 48h
Gender according to drug classes ingestion
Pourcentage of gender compared according drug classes ingestion
Time frame: 48h
Time (median) of admission according to drug classes ingestion
Time frame: 48h
Time (median) of admission according unit of admission
Time frame: 48h
Mortality according to drug class ingestion
Time frame: 30 days
ICU admission according to drug class ingestion
Time frame: 30 days
icu admission (percentage)
Time frame: 48h
percentage of errors according to the Grenoble clinical decision rule
Time frame: 30 days
multivariate analysis to describe factors associated with ICU admission
Time frame: 30 days
multivariate analysis to describe factors associated with mobile intensive care unit dispatch
Time frame: 30 days
No study locations are listed for this record.
This study is completed, as verified in Apr 2019. You cannot join it, but the record below documents what was studied.
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University Hospital, Grenoble