CompletedNot Applicable

Post-ICU Consultation : a Time to Discuss Advance Directives (CoPRADA)

France40 participantsStarted 2021-12-09

Plain-language summary

The aim of this study is to assess the possibility of discussing advance directives during post-intensive care consultation.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients with 48 hours of mechanical ventilation * Patients with a 5 days stay in ICU Exclusion Criteria: * Patients with therapeutic limitation discussed during their ICU stay * Geographical remotness to come to the post-ICU consultation * Minor patients * Patient not affiliated to the social security scheme

What they're measuring

Number of patients willing to discuss AD after an ICU stay

Timeframe: 1 year

Trial details

NCT IDNCT05817500

SponsorUniversity Hospital, Brest

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2022-12-09

View on ClinicalTrials.gov More Advance Directives trials