No intervention
Otherobservational study, no intervention performed
NCT Number: NCT05108792
This research is a descriptive observational study conducted in multicenter (intensive care and continuing care units) in France. All data collected is part of the patient record. The main objective is to describe the end-of-life sedative practices following a decision to limit or stop therapy in intensive care unit and continuing care unit.
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Notify Me18 year and older
All sexes
Observational
CHU Amiens, Amiens, France
All participating sites will include last 10 consecutive major patients deceased following a decision to limit or stop therapeutics. The study include only data from patients died before January 1, 2020. In the case report form the following information will be entered:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
observational study, no intervention performed
Time frame: after patient death (before january 1st 2020)
Information concerning end-of-life sedative practices are recorder in the CRF (treatments used, patient's and unit characteristics...)
Société Française d'Anesthésie et de Réanimation
Other
Continuous Deep Sedation Until Death Following a Decision to Limit or Stop Treatment in Intensive Care and in Continuous Surveillance Units
Acronym: SPCMD-REA
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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