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NCT06866366Completed

Retrospective, Multicenter, Single-arm, Observational Study, With Data From Patients With T2DM With Malnutrition or at Risk, Who Were Prescribed Resource® Diabet Plus as a Hypercaloric and Hyperproteic Specific Formula for Patients With T2DM

Impact of the Use of Resource® Diabet Plus on Metabolic Control in Patients With T2DM Who Are Malnourished or at Risk of Malnutrition

Source: ClinicalTrials.gov · Last updated 7 Oct 2025

Brief summary (registry, in English)

This retrospective multicentre study aims to provide real-world evidence of the effectiveness of Resource® Diabet Plus as supplementation tool for T2DM patients with malnutrition or at risk of malnutrition, under conditions of routine clinical practice in Spain.

Status (registry)
Completed
Study type
Observational
Enrollment
59 (actual)
First submitted
4 Mar 2025
Start date
23 Apr 2025
Primary completion date
13 Jul 2025
Lead sponsor
Outcomes'10
NCT number
NCT06866366

What you commit to

  • Study type: Observational
  • Participants enrolled: 59
  • From 23 Apr 2025 to the primary completion date, 13 Jul 2025
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with severe renal insufficiency (glomerular filtration rate \< 30mL/min/1.73m2) at the time of selection.

Other

  • Pregnant or breastfeeding women.
  • Patients who required any other type of nutritional supplementation during the study period (parenteral/enteral).

Who the study is looking for

  • 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.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hospital Universitario Insular de Gran Canaria
Coordinator of this site? Confirm its status
Las Palmas de Gran CanariaSpainUnknown status
Hospital Clínico Universitario Virgen de la Arrixaca
Coordinator of this site? Confirm its status
MurciaSpainUnknown status
Hospital Universitario Nuestra Señora de la Candelaria
Coordinator of this site? Confirm its status
Santa Cruz de TenerifeSpainUnknown status
Hospital Universitario Virgen Macarena
Coordinator of this site? Confirm its status
SevilleSpainUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.