Status:
COMPLETED
Study in Intensive Care Follow-up Programme in Improving Long-term Outcomes of ICU Survivors
Lead Sponsor:
Assistance Publique - Hôpitaux de Paris
Conditions:
Quality of Life
Post ICU Discharge
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Study Hypothesis: Critical illness is associated with long-term medical and psychological sequelae that can impact the professional and private life. The purpose of the present multicenter randomized...
Detailed Description
Critically ill patients who had required at least 3 days of mechanical ventilation and who consented to participate will be randomized at time of ICU discharge in either follow-up or not follow-up arm...
Eligibility Criteria
Inclusion
- Men and women older than 18
- Living in an area near the hospital
- Hospitalized in the ICU medical surgical hospitals in this study.
- Who required mechanical ventilation more than 3 days
- Having a life expectancy greater than one year (Mc Cabe score \>2, absence of metastatic cancer)
- Having a general practitioner identified
- Is affiliated to a social health care
- And who have given their written informed consent
Exclusion
- Patients hospitalized in ICU in the previous year
- Patients followed for a preexisting myopathy
- The burn patients, patients with brain injury (Glasgow initial \<8) or trauma
- Patients hospitalized for suicide or self-induced poisoning
- Patients with psychiatric disorders
- Patients with ore dementia
- Pregnant women
- Patients who do not speak fluently French
- Patients with guardianship
- Homeless patients
- No having a general practitioner identified
Key Trial Info
Start Date :
December 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 11 2020
Estimated Enrollment :
545 Patients enrolled
Trial Details
Trial ID
NCT01796509
Start Date
December 1 2012
End Date
March 11 2020
Last Update
January 5 2022
Active Locations (1)
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1
Hôpital Raymond Poincaré
Garches, Île-de-France Region, France, 92380