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Impact of Socio-economic Vulnerability on Initial Severity and Prognosis in Patients Admitted to an ICU. (IVOIRE)

U

University Hospital Center (CHU) Dijon Bourgogne

Status

Completed

Conditions

Patients at Intensive Care Unit

Treatments

Other: Quality of life questionnaires

Study type

Interventional

Funder types

Other

Identifiers

NCT01907581
Quenot PHRC IR 2012

Details and patient eligibility

About

A gravity admission largest resuscitation and a poorer prognosis are expected for patients experiencing socio-economic vulnerability. This is the first study in France and investigating the field of resuscitation which will allow us to have a vision of the French health system and its consequences. The frequency of PTSD is expected to be more important in this vulnerable population itself with quality of life at discharge worse. The results of this study are a prerequisite for the implementation of preventive measures targeted and more suitable for those patients experiencing socio-economic vulnerability remediation.

Enrollment

1,417 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient who have been informed about the study (directly or via a person of trust) and have given their consent
  • Patients admitted to intensive care in accordance with the criteria defined by decree n° 2002-465 of the law of 05th April 2002 relative to the rights of patients and the quality of the healthcare system. It concerns patients who present or are likely to present life-threatening acute multi-organ failure requiring support care involving at least one of the following procedures: invasive or non-invasive mechanical ventilation, continuous or discontinuous hemofiltration, dobutamine, adrenaline, noradrenaline, ECMO

Exclusion criteria

    • Refusal to take part,
  • Age < 18 years
  • Adult under guardianship (or ward of court),
  • Patients impossible to follow for 3 months (concomitant disease not related to the admission to the ICU that may cause death within 3 months....),
  • Patients presenting major cognitive impairment that precludes a reliable interview,
  • Patients and/or close relatives/friends who cannot be questioned or cannot provide information,
  • Absence of a family and/or close friends

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

1,417 participants in 1 patient group

Patients admitted to an ICU
Other group
Treatment:
Other: Quality of life questionnaires

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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