Coverage of Requirements After Consumption of a Nutritional Formula in Patients With Chewing/Swal… (NCT03727191) | Clinical Trial Compass
CompletedNot Applicable
Coverage of Requirements After Consumption of a Nutritional Formula in Patients With Chewing/Swallowing Problems.
Spain60 participantsStarted 2018-05-01
Plain-language summary
Effect of a nutritional formula on the nutritional requirements in patients with chewing/swallowing problems during one month
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Men and women over 18 years old.
* Individuals with chewing/swallowing disorder.
* Individuals well nourished or at malnutrition risk.
* Adequate cultural level and understanding of the clinical trial.
* Signed informed consent.
Exclusion Criteria:
* Individuals with body mass index ≥40 kg/m2.
* Individuals with acute, severe or chronic disease without control.
* Individuals with major surgeries during the last month.
* Individuals with gastrointestinal surgery the last three months.
* Individuals with moderate/severe cognitive impairment.
* Individuals with severe malnutrition.
* Individuals with amyotrophic lateral sclerosis.
* Individuals who consume nutritional oral supplements seven days prior to the start of the study.
* Enteral or parenteral nutrition.
What they're measuring
1
Percentage of nutritional changes with regard to the nutritional requirements recommended
Timeframe: Up to one month
Trial details
NCT IDNCT03727191
SponsorInstituto de Investigación Hospital Universitario La Paz