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
- Diseases
- Crohn's disease, Ulcerative colitis
- 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
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| AOU Federico II Coordinator of this site? Confirm its status | Naples | Italy | Recruiting |
| IRCCS Policlinico San Matteo, Pavia Coordinator of this site? Confirm its status | Pavia | Italy | Recruiting |
| Ospedale Isola Tiberina - Gemelli Isola Coordinator of this site? Confirm its status | Roma | Italy | Recruiting |
| IRCCS Humanitas Coordinator of this site? Confirm its status | Rozzano | Italy | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.