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NCT Number: NCT01766531

Evaluation of Nutritional Status in ICU : Interest for the Measurement of Body Composition by Body Bioelectrical Impedance and Comparison With Several Methods

Prospective cohort, monocentric non-randomized and interventional clinical study in ICU assessing the evolution of body composition using bioelectrical impedance analysis.

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Key information

Conditions

Body Composition

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

CHU Clermont-Ferrand

Clermont-Ferrand, 63003, France

About this study

Prospective, monocentric non-randomized and interventional clinical study in ICU assessing the evolution of body composition using bioelectrical impedance analysis (phase angle, fat mass, muscle mass, fat-free mass, body water); comparison with four methods for assessing nutritional status. ; compare length of mechanical ventilation, length in ICU and energy expenditure rest between malnourished and non-malnourished patient.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ICU patients
  • Written informed consent
  • Adult patient

Exclusion criteria

  • Pregnant patient
  • Cardiac -pacemaker

Treatment and study plan

body bioelectrical impedance

Device

Primary outcomes

  1. Evolution of fat-free mass

    Time frame: From day 4 to day 7

  2. Evolution of fat-free mass

    Time frame: from day 8 to day 14

  3. Evolution of fat-free mass

    Time frame: from day 14 to day 28

Secondary outcomes

  1. Performance of the impedance to measure body evolution

    Time frame: in the first three days, from day 4 to day 7, from day 8 to day 14, from day 14 to day 28

  2. Evolution of phase angle using bioelectrical impedance analysis

    Time frame: in the first three days, from day 4 to day 7, from day 8 to day 14, from day 14 to day 28

  3. Comparison with four methods for assessing nutritional status

    Time frame: in the first three days, from day 4 to day 7, from day 8 to day 14, from day 14 to day 28

  4. Compare length of mecanical ventilation, length in ICU and energy expenditure rest between malnourished ans non-malnourished patient

    Time frame: in the first three days, from day 4 to day 7, from day 8 to day 14, from day 14 to day 28

Sponsors and collaborators

Lead sponsor

University Hospital, Clermont-Ferrand

Other

Collaborators

  • Center of study in Human Nutrition, INRA, Department of Clinical Nutrition

Registry information

Acronym: IMPREA

Important dates

Study start
2012
Primary completion
2012
Study completion
2012
First posted
Jan 11, 2013
Registry last updated
Dec 2, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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