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The CONFUCIUS Oral Protein Supplementation Trial — CONFUCIUS  

Critical Illness Clinical Trial

Official title:
CONvalescence of FUntional Outcomes After ICU Stay by Oral Protein Supplementation

Clinical Trial Summary

Study the effect of 6-weeks porcine protein supplementation vs isocaloric comparator (carbohydrate) on functional outcomes in post ICU-patients. Patients will be included at ICU discharge. Included patients will receive the supplements twice daily (morning and afternoon), starting at the first day at the general ward. To the best of our knowledge, a study on protein supplementation in the post-ICU period to address its effect on functional outcomes is lacking.

Clinical Trial Description

Patients discharged from the Intensive Care Unit frequently suffer from Post Intensive Care Syndrome. This syndrome is characterized by muscle weakness and physical disabilities besides neurocognitive and psychological disturbances. Studies have shown that protein requirements in the post-ICU phase are often not met. Furthermore, protein supplementation in other patient groups have shown beneficial effects. However, a study on protein supplementation during the post-ICU period is lacking. This study aims to investigate the effect of protein supplementation on functional outcomes in post-ICU patients. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05405764
Study type Interventional
Source Gelderse Vallei Hospital
Contact Arthur RH van Zanten, MD, PhD
Phone 318434115
Email zantena@zgv.nl
Status Recruiting
Phase N/A
Start date April 19, 2022
Completion date April 30, 2024
View Details
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