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

NCT05817500 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2023-04-18

No results posted yet for this study

Summary

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

Conditions

  • Advance Directives
  • Post Intensive Care Syndrome
  • Advance Care Planning

Sponsors & Collaborators

  • University Hospital, Brest

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-12-09
Primary Completion
2022-12-09
Completion
2022-12-09

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05817500 on ClinicalTrials.gov