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Influence Of Nutritional Status Of Patients In The Intensive Care Output On Long Term Fate

Influence Of Nutritional Status Of Patients In The Intensive Care Output On Long Term Fate

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01750671
Acronym
FEEDING
Enrollment
680
Registered
2012-12-17
Start date
2012-12-31
Completion date
2015-12-31
Last updated
2012-12-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nutritional Status at the Release of ICU.

Keywords

ICU, Body composition, Nutrition, Survival, Morbidity

Brief summary

It is established that the surviving patients after a stay in the ICU are characterized by frequent malnutrition and morbidity and mortality. The main goal of this work is to study the relationship between nutritional statuses during ICU hospitalization, whatever its determinants, and quality of life, morbidity and mortality at one year. The hypothesis of the study is that the presence of under nutrition is responsible for a 10% increase in crude mortality at one year (which would be respectively 30% for malnourished patients and 20% for non-malnourished patients).

Detailed description

This is a multicenter cohort study of a 30-month follow-up on patients after a stay in ICU. Nutritional parameters and evaluation of the quality of life will be collected during hospitalization and output during a visit to the Clinical Research Associate at 6 months and one year. Survival will be also noted. These parameters will be studied in comparative patients malnourished and non-malnourished.

Interventions

None listed

Sponsors

Société des Produits Nestlé (SPN)
CollaboratorINDUSTRY
Baxter S.A.S
CollaboratorUNKNOWN
University Hospital, Strasbourg, France
CollaboratorOTHER
Hospices Civils de Lyon
CollaboratorOTHER
University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Study design

Observational model
COHORT

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients of both sexes, age greater than or equal to 18 years * Hospitalized more than 72 hours in the ICU * Requiring at least one support organ failure: 1. Ventilatory support (invasive or noninvasive) 2. Administration of catecholamines 3. Extrarenal purification whatever technique * Affiliated to a social security system * Having given free, informed written consent

Exclusion criteria

* Patients with end-stage disease or for which a limitation of care was decided * Pregnant women * Patients with minor or under guardianship * Incapacitated adults and psychiatric inpatients

Design outcomes

Primary

MeasureTime frame
all-cause mortalityat one year

Secondary

MeasureTime frame
Post-traumatic stressat inclusion, M6 and M12
Quality of lifeat M6 and M12
Degree of activity (Karnofsky questionnaire)At M6 and M12
Weightat inclusion, M6 and M12
Anxiety and depressionat inclusion, M6 and M12
Albuminat inclusion, M6 and M12
Orosomucoidat inclusion, M6 and M12
Transthyretin (prealbumin)at inclusion, M6 and M12
Body compositionat inclusion, M6 and M12
Body mass indexat inclusion, M6 and M12

Countries

France

Contacts

Primary ContactPatrick LACARIN
placarin@chu-clermontferrand.fr04 73 75 11 95

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026