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NCT03230448 Clinical Trial

Study of the Links Between Suicidal Intentionality and Acute Alcoholism

Suicide, Attempted Clinical Trial

— ISA  

Official title:
Study of the Links Between Suicidal Intentionality and Acute Alcoholism

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03230448
Other study ID # RC31/17-0074
Secondary ID 2017-A00641-52
Status Completed
Phase N/A
First received July 24, 2017
Last updated August 30, 2017
Start date May 29, 2017
Est. completion date July 31, 2017

Study information
Verified date August 2017
Source University Hospital, Toulouse
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

There is a strong link between the alcohol consumption and the suicidal risk. Indeed there is an increase of the risk of suicide in case of chronic or acute alcohol consumption. However why the alcohol consumption increase the suicidal risk is unknown.

The hypothesis of this study is that the alcohol consumption induced disinhibition and facilitates the suicide attempt without premeditation

Description:

People hospitalized after a suicide attempt will answer to two questionnaires about the suicide intentionality and the acute alcohol consumption.

There is 2 arms:

people doing suicide attempt and with positive level of alcohol (up to 0.1g.L) people doing suicide attempt and with negative level of alcohol

110 patients will be included in this study so 55 in each arm.

Recruitment information / eligibility
Status Completed
Enrollment 110
Est. completion date July 31, 2017
Est. primary completion date July 31, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patient hospitalized in emergency department for a suicide attempt by voluntary drug intoxication

- speaking and understanding french

Exclusion Criteria:

- Patient who has used other psychoactive substances (attested by toxicological analyzes and / or interrogation)

- Known neurodegenerative pathology

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• questionnaire
after the inclusion patient will answer to a questionnaire about the suicidal intentionality and a second about the alcool consumption

Locations
Country Name City State
France University Hospital of Toulouse Toulouse

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Toulouse

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary compare the score of suicidal intentionality in patient presenting a positive or a negative alcohol level and doing suicide attempt patient will complete the PIERCE questionnaire about the suicidal intentionality 15 minutes
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