Menu
Not yet recruiting NCT07417592

Study on the Priorities of Patients Admitted to Intensive Care

— Observational Intensive Care Unit Syndrome

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Intensive Care Unit Syndrome. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The goal of this observational study is to learn about the priorities of patients admitted to intensive care units (ICUs) who have a life-threatening condition, as well as the priorities assumed by their designated relatives and healthcare professionals (nurses, nursing assistants, ICU physicians, and general practitioners).

Primary outcome measures

  • Agreement rate [Time frame: 48 hours]

Eligibility criteria

Inclusion criteria for Patient:

  • Adult Patient
  • Estimated length of stay in intensive care exceeding 72 hours
  • No objection from the patient or the designated representative, if the patient is unable to consent to participate in the study

Inclusion criteria for Designated representative:

  • Adult Person
  • No objection to participate in the study

Inclusion criteria for Caregiver:

  • No objection to participate in the study

Exclusion criteria

  • Patients under legal protection (guardianship, conservatorship)
  • Pregnant or breastfeeding women
  • Disagreement among the patient's relatives regarding the designated representative.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

France · 1 center
  • CHU de Brest — Brest

Identifiers

NCT: NCT07417592 · 29BRC25.0322 · 2025-A02336-43

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗