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| ID | Type | Description | Link |
|---|---|---|---|
| 2021-002329-56 | EudraCT Number |
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Critically ill patients are known to develop serious nutritional deterioration during the course of their disease. They develop, from the beginning, a multifactorial protein malnutrition that relates to a poor clinical course and the development of weakness. Due to the increased protein catabolism in this type of patient, there is a rapid degradation of muscle mass and loss of functional proteins, and therefore nutritional support is mandatory. Indeed, achieving a high protein intake may promote a better evolution of the critically ill patient, i.e., maintenance of muscle protein, less deterioration of muscle strength, lower Intensive care unit-acquired weakness (ICUAW), lower mortality, decrease in the number of infections, decrease in days on mechanical ventilation, and days of hospital stay and in ICU.
The goal of this clinical trial is to compare the appearance and degree of ICUAW in critically ill patients receiving invasive mechanical ventilation treated with two different doses of protein (1.5 g/kg/day vs.1.0 g/kg/day).
It is known that protein metabolism is altered in critically ill patients due to metabolic alterations derived from stress. This critical situation is manifested by a severe catabolic alteration, especially in the first week, which is fundamentally characterized by severe glucose intolerance and the use of the protein itself as a metabolic substrate.
Despite protein synthesis is increased, this is insufficient to compensate for the high protein degradation rate, which leads, among others, to muscle deterioration resulting in increased morbidity and mortality. This muscle destruction has been implicated in the early appearance of Intensive care unit-acquired weakness (ICUAW). Although the pathophysiology of ICUAW is multifactorial, protein intake may play an key role in its treatment. However, protein intake cannot reduce muscle destruction, but it can stimulate protein synthesis.
Current evidence supports that the administration of early artificial nutritional support with a high protein intake can improve the clinical course of critically ill patients. However, there is still no consensus on the exact amount of protein needed to be administered to these patients in order to reduce adverse outcomes and prevent ICUAW.
Thus the aim of this study is to evaluate the effect of a nutritional supplementation containing 1.5 g of protein/kg/day vs 1.0 g of protein /kg/day in critically ill patients receiving mechanical ventilation on the development and degree of ICUAW.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Protein dose 1.5 g/kg/day | Experimental | Administration of 1.5 g of protein/kg/day in critically ill patients receiving invasive mechanical ventilation |
|
| Protein dose 1.0 g/kg/day | Active Comparator | Administration of 1.0 g of protein/kg/day in critically ill patients receiving invasive mechanical ventilation |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Protein dose 1.5 g/kg/day | Other | Administration of 1.5 g of protein/kg/day via enteral/parenteral nutrition |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change of intensive care unit acquired weakness (ICUAW). | Determined by Medical Research Council sum score (MRC-SS). Diagnosis of ICUAW if MRC-SS < 48 (maximun score 60). | Baseline, weekly in ICU up to 28 days after mechanical ventilation termination, throughout hospital stay, an expected average of 6 weeks, and 90 days after hospital discharge. |
| Measure | Description | Time Frame |
|---|---|---|
| Muscle Strength. | Dynamometry. | Up to 6 months. |
| Active mobility. | Determined by Intensive Care Unit Mobility Scale (ICUMS). Scored from 0 to 10 being 0 no activity, lying in bed, and 10 walking independently without a gait aid. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| María Carmen Sánchez Álvarez, PhD | Sociedad Española de Medicina Intensiva, Crítica y Unidades Coronarias (SEMICYUC) | Principal Investigator |
| Juan Francisco Fernández Ortega, PhD | Hospital Regional de Malaga | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hospital Universitario Germans Trias i Pujol | Badalona | Barcelona | 08916 | Spain | ||
| Hospital Universitario de Bellvitge |
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Within 48 hours, intensive care patients on expected invasive mechanical ventilation of at least three days are allocated into two groups receiving enteral/parenteral nutrition with 1.5 g of protein/kg/day or 1.0 g of protein/kg/day as an active comparator.
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| Protein dose 1.0 g/kg/day | Other | Administration of 1.0 g of protein/kg/day via enteral/parenteral nutrition |
|
| Up to 6 months. |
| Nosocomial infections. | Centers for disease control and prevention (CDC). | Throughout hospital stay, an expected average of 6 weeks. |
| Mechanical ventilation. | Number of days receiving mechanical ventilation. | Up to 1 month. |
| Gastrointestinal complications. | Gastric residual volume, diarrhea, vomiting or regurgitation, abdominal distension, constipation. | Throughout hospital stay, an expected average of 6 weeks. |
| Metabolic complications. | Glycemia, fluid intake, electrolytes/trace element determination, hypertriglyceridemia, liver disfunction, cholestasis, necrosis or mixed dysfunction, overfeeding. | Throughout hospital stay, an expected average of 6 weeks. |
| Mortality rate. | Number of deaths/total participants | Up to 6 months. |
| Length of ICU and hospital stay. | Number of days of hospitalization. | Throughout hospital stay, an expected average of 6 weeks. |
| Quality of life index. | European Quality of Life-5 Dimensions (EQ-5D). Scored from 0 to 100 being 0 the worst health imaginable and 100 the best health imaginable. | Up to 6 months. |
| L'Hospitalet de Llobregat |
| Barcelona |
| 08907 |
| Spain |
| Hospital General Universitario de Castellón | Castellon | Castelló | 12004 | Spain |
| Hospital Universitario de Badajoz | Badajoz | Extremadura | 06080 | Spain |
| Hospital de Barbastro | Barbastro | Huesca | 22300 | Spain |
| Hospital Universitario de Fuenlabrada | Fuenlabrada | Madrid | 28942 | Spain |
| Hospital Universitario Infanta Cristina | Parla | Madrid | 28981 | Spain |
| Hospital de Manacor | Manacor | Mallorca | 07500 | Spain |
| Hospital General Universitario Santa Lucía | Cartagena | Murcia | 30202 | Spain |
| Hospital Clínico Universitario Virgen de la Arrixaca | El Palmar | Murcia | 30120 | Spain |
| Hospital General Universitario Los Arcos del Mar Menor | Pozo-Aledo | Murcia | 30739 | Spain |
| Hospital Universitario Doctor Josep Trueta | Girona | 17007 | Spain |
| Hospital Universitario Clínico San Cecilio | Granada | 18016 | Spain |
| Hospital Universitario San Jorge | Huesca | 22004 | Spain |
| Hospital Universitario 12 de Octubre | Madrid | 28041 | Spain |
| Hospital Universitario La Paz | Madrid | 28046 | Spain |
| Hospital Universitario Regional de Málaga | Málaga | 29010 | Spain |
| Hospital General Universitario Morales Meseguer | Murcia | 30008 | Spain |
| ID | Term |
|---|---|
| D016638 | Critical Illness |
| D006963 | Hyperphagia |
| ID | Term |
|---|---|
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D012817 | Signs and Symptoms, Digestive |
| D012816 | Signs and Symptoms |
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