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NCT07433946Recruiting

Partial Enteral Nutrition to Prevent Weight Loss and Sarcopenia in IBD Patients at Nutritional Risk - SIMBA

Partial Enteral Nutrition Effects on Weight Loss and Sarcopenia in Patients With IBD at Risk of Caloric-Protein Malnutrition - SIMBA

Source: ClinicalTrials.gov · Last updated 25 Jun 2026

Brief summary (registry, in English)

This is a multicenter, open-label, randomized two-arm interventional nutritional study evaluating the effects of partial enteral nutrition (LH VIOLA) in patients with Inflammatory Bowel Disease (IBD) at risk of malnutrition. A total of 146 patients (73 per arm) will be enrolled across 4 centers. IBD, including Crohn's Disease and Ulcerative Colitis, is associated with malabsorption, weight loss, sarcopenia, and malnutrition, which negatively impact quality of life and treatment outcomes. Nutritional assessment using the Malnutrition Universal Screening Tool (MUST) will identify patients at risk. Participants will be randomized to receive either nutritional counseling alone or counseling plus oral LH VIOLA supplementation (≥412 kcal/day) for 16 weeks. The primary objective is to evaluate maintenance or recovery of body weight at 16 weeks. Secondary objectives include assessment of weight at 24 weeks, muscle strength (handgrip), body composition and metabolic parameters (BIA/BIVA, vitamin B12/D, pre-albumin), quality of life (SF-12), economic impact, adherence, gastrointestinal tolerability, and reduction in malnutrition risk (MUST score). The study duration per patient is 24 weeks (16 weeks of intervention plus 8 weeks follow-up), with a total study duration of 18 months. The sample size is powered to detect an increase from 40% to 65% in patients achieving weight maintenance or gain at 16 weeks, accounting for a 15% dropout rate.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
146 (estimated)
First submitted
19 Feb 2026
Start date
Mar 2026
Primary completion date
Dec 2026
Lead sponsor
Lionhealth Srl Società Benefit
NCT number
NCT07433946

What you commit to

  • Study type: Interventional
  • Planned participants: 146
  • From Mar 2026 to the primary completion date, Dec 2026
  • 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

  • Following an exclusion diet (CDED)
  • Current hospitalization
  • Pregnancy
  • Requirement for a low-protein diet

Who the study is looking for

  • Age 18-65 years
  • Diagnosis of Crohn's Disease or Ulcerative Colitis
  • At risk of malnutrition according to the Malnutrition Universal Screening Tool (MUST)
  • Ability to provide informed consent
  • Women of childbearing potential must use effective contraception

Age in the registry: 18 years to 65 years · 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
AOU Federico II
Coordinator of this site? Confirm its status
NaplesItalyRecruiting
IRCCS Policlinico San Matteo, Pavia
Coordinator of this site? Confirm its status
PaviaItalyRecruiting
Ospedale Isola Tiberina - Gemelli Isola
Coordinator of this site? Confirm its status
RomaItalyRecruiting
IRCCS Humanitas
Coordinator of this site? Confirm its status
RozzanoItalyRecruiting

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