Actively Recruiting
Nutritional Therapy in Patients With Post-extubation Dysphagia
Led by National Institute of Respiratory Diseases, Mexico · Updated on 2024-07-19
128
Participants Needed
1
Research Sites
178 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this study is to evaluate the impact of the prescription of two doses of protein on the amount in kilograms of muscle mass and on the clinical evolution (time until safe swallowing, time until removal of the feeding stoma, number of hospital readmissions, feeding stoma infections, incidence of pneumonia, functionality, number of falls, fractures and mortality) at 6 months after hospital discharge in patients with enteral nutrition due to post-extubation dysphagia.
CONDITIONS
Official Title
Nutritional Therapy in Patients With Post-extubation Dysphagia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who required invasive mechanical ventilation during their hospital stay with a diagnosis of post-extubation dysphagia diagnosed by fibroendoscopy evaluation of swallowing (FEES).
- Patients discharged with a feeding tube.
- Patients with signed informed consent.
You will not qualify if you...
- Patients with pre-existing dysphagia or neurological conditions that can cause dysphagia (e.g., multiple sclerosis, Parkinson's disease, Alzheimer's, myasthenia gravis).
- Patients with chronic kidney disease, defined as a glomerular filtration rate <60 ml/min.
- Patients discharged with a terminal condition and/or life expectancy less than 3 months.
- Diagnosis of HIV, under clinical follow-up by a specialist team.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
National Institute of Respiratory Diseases
Mexico City, Mexico, 14080
Actively Recruiting
Research Team
I
Ivan A Osuna-Padilla, PhD
CONTACT
A
Alan Garcia-Grimaldo, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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