Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 4:01 PM
Ignite Modification Date:
2025-12-24 @ 4:01 PM
NCT ID:
NCT06866366
Eligibility Criteria:
Inclusion Criteria:
* Patients ≥ 18 years.
* Outpatients or hospitalised patients, at discharge with a diagnosis of type 2 Diabetes.
* Patients at risk of malnutrition detected by validated screening tools or with DRM diagnosed by GLIM criteria.
* Patients who have been prescribed 1-2 bottles/day of Resource® Diabet Plus following the conditions of use of its technical data sheet, in the last 2 years, with at least 24 weeks of evolution recorded in the clinical history.
* Patients who have Hb1Ac data in the medical record on the index date and during evolution.
Exclusion Criteria:
* Pregnant or breastfeeding women.
* Patients who required any other type of nutritional supplementation during the study period (parenteral/enteral).
* Patients with severe renal insufficiency (glomerular filtration rate \< 30mL/min/1.73m2) at the time of selection.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06866366
Study Brief:
Protocol Section:
NCT06866366