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

R

Regional University Hospital Center (CHRU)

Status

Completed

Conditions

Advance Care Planning
Post Intensive Care Syndrome
Advance Directives

Study type

Observational

Funder types

Other

Identifiers

NCT05817500
29BRC21.0335 - CoPRADA

Details and patient eligibility

About

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

Full description

After a stay in intensive care units (ICU), patients can experience physical, psychological and cognitive impairments. To assess this post intensive care syndrom (PICS), post-ICU consultation have been developed.

Since 5 year mortality is higher in ICU survivors, it might be interesting to address those patients' views relating to illness and end of life through a discussion on advance directives (AD), during post-ICU consultation.

However, the development of these consultations being recent, it has not yet been assessed whether this consultations might be a suitable time to discuss AD and the intensivit a suitable interlocutor.

Enrollment

40 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

40 participants in 1 patient group

ICU patients with > 48h mechanical ventilation and/or > 5 days stay in ICU

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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