- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02843776
Requests for Euthanasia and Assisted Suicide (EPIDESA2)
July 16, 2018 updated by: Centre Hospitalier Universitaire de Besancon
Requests for Euthanasia and Assisted Suicide : Epidemiological Study Conducted as Part of the Establishment of a Structured Network
The study epiDESA2 identifies all explicit requests for euthanasia or assisted suicide expressed by the person him/herself, regardless of which professional is asked and regardless of where the request is made (primary care, health institutions, medico-social institutions including nursing home care or at home) in the Burgundy-Franche-Comté region during six months.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
65
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Besancon, France, 25000
- CHRU Besançon
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The study epiDESA2 identifies all explicit requests for euthanasia or assisted suicide expressed by the person him/herself regardless of where the request is made (primary care, health institutions, medico-social institutions including EHPADs or at home) in the regions of Burgundy-Franche-Comté during six months.
Description
Inclusion Criteria:
Any adult :
- Living at home, or in medico-social institutions or hospitalized in primary care or health institutions of Burgundy-Franche-Comté,
- At the end of life due to advanced stage disease or a major change in the state of health of an elderly person,
- Who expressed an explicit request for euthanasia or assisted suicide,
- Who expressed their no objection to the collection of their datas,
- Who are covered by the French social security system.
Exclusion Criteria:
- They are underage
- The request was expressed by another person
- The request is not an explicit request
- The request appears in the context of a situation other than illness or a general change in state of health
- The patient is mentally confused
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Census of requests for euthanasia or assisted suicide in Burgundy-Franche-Comté
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2017
Primary Completion (Actual)
December 31, 2017
Study Completion (Actual)
December 31, 2017
Study Registration Dates
First Submitted
July 19, 2016
First Submitted That Met QC Criteria
July 21, 2016
First Posted (Estimate)
July 26, 2016
Study Record Updates
Last Update Posted (Actual)
July 17, 2018
Last Update Submitted That Met QC Criteria
July 16, 2018
Last Verified
July 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- EPIDESA2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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