Clinical Trials Directory

Trials / Recruiting

RecruitingNCT04348318

Advance Directive Implementation and Scientific Evaluation Study

Advance Directive Implementation and Scientific Evaluation (ADVISE) Study

Status
Recruiting
Phase
Study type
Observational
Enrollment
2,000 (estimated)
Sponsor
University Hospital, Basel, Switzerland · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is to better understand the use of advance directives, their implementation in the intensive care unit, and their effects on outcome. Data from the digital medical records of all consecutive adult patients admitted to the intensive care unit at the University Hospital Basel from 2011 to 2023 are retrospectively extracted. Descriptive analyses will be applied to report the proportion of patients with an advance directive. In-hospital outcome (defined as survival, Glasgow Outcome Score, and return of neurologic function to premorbid baseline) will be compared between patients with and without advanced directives

Conditions

Interventions

TypeNameDescription
OTHERhealth related personal data extraction from digital medical recordshealth related personal data extraction from digital medical records (i.e. patient characteristics; start, end and duration of hospitalization and ICU stay; admitted from another hospital, nursing home or comes with emergency medical Service; formal data of written advance directives; data of unwritten advance directive; information on the contents of the advance directives (regarding life-worthy conditions, health care agents, resuscitation, pain management, artificial nutrition, hydration, surgeries, renal replacement, mechanical circulation, mechanical ventilation, pacemaker, administration of blood products, treatment of infections, organ donation, autopsy); patient history; clinical data; therapeutic features; outcome at discharge; knowledge regarding relatives and their level of information about the advance directives; discussion of euthanasia and self-determination of dying.

Timeline

Start date
2021-08-03
Primary completion
2050-12-01
Completion
2050-12-01
First posted
2020-04-16
Last updated
2025-02-14

Locations

2 sites across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT04348318. Inclusion in this directory is not an endorsement.