About this trial
In this pilot observational study the primary outcome is to assess, in a Respiratory Rehabilitation Unit, if there is an association between sarcopenia, assessed by handgrip strenght and BIA, and a delayed decannulation time in patients who underwent tracheostomy.
Secondary outcomes are to assess if there is an association between an increased malnutrition risk (assessed by MUST), a poor nutritional status (assessed by GLIM criteria) and a delayed decannulation time and the gut microbiota composition.
Eligibility criteria
Qualifiers
Signed informed consent from patients or legal guardians for patients unfit to plead
Presence of tracheostomy at admission
Disqualifiers
Refusal
Pregnancy
Pace maker/implantable cardioverter
No legal guardians for patients unfit to plead
Trial design
Treatments tested in this trial
- handgrip strenght
- Bioelectrical Impedance Analysis (BIA)
- MUST
- GLIM
- Gut microbiota
- Blood Sample
- Anthropometric measures
Treatment groups
Sponsors and collaborators
Fondazione Don Carlo Gnocchi Onlus
Lead sponsor
University of Florence
Collaborator