NCT06781619 Effect of Plant Based High Energy High Protein Oral Nutritional Supplement on Nutritional Intake in Patients With or at Risk of Disease Related Malnutrition.
| NCT ID | NCT06781619 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Nutricia Research |
| Condition | Disease Related Malnutrition |
| Study Type | INTERVENTIONAL |
| Enrollment | 80 participants |
| Start Date | 2025-03-17 |
| Primary Completion | 2026-09 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 80 participants in total. It began in 2025-03-17 with a primary completion date of 2026-09.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The subjects will use study product twice daily for 8 weeks starting at Visit 1. The recommendation is to consume one serving in the morning and one in the afternoon / evening between meals. The duration of the study for each subject will be approximately 11 weeks, comprising a screening period of max 2 weeks, an intervention period of 8 weeks, and a follow up phone call 1 week after completion of the intervention. A blood sample will be drawn at visit 1 and visit 3.
Eligibility Criteria
Inclusion Criteria: 1. Age ≥ 18 years 2. Identified as at medium or high risk of malnutrition based on: 1. MUST score ≥ 1 and / or 2. Being prescribed with ONS and willing and able to switch from pre-study prescribed ONS to the Test or Control Product for participation in the study 3. In need of 2 servings of ONS/day (400 kcal; 20 gr protein per serving) for at least 8 weeks as determined by the treating healthcare professional. 4. Medically and physically able to consume high energy high protein ONS in the opinion of the Investigator. 5. Willing to maintain dietary habits for the duration of the study. 6. Willing to consume plant based as well as dairy based ONS Exclusion Criteria: 1. Known allergy to soy, cow's milk protein or to any other ingredients as listed in the study product composition (refer to the product information brochure (PIB) and the appendix of this protocol). 2. Known intolerance to any ingredients as listed in the study product composition (refer to PIB and appendix of this protocol). Subjects with lactose intolerance who use lactase may still be enrolled in the study. 3. Any contraindication to oral feeding per se, including gastrointestinal failure or suppressed gastrointestinal function, complete intestinal obstruction and major intraabdominal sepsis. 4. Active flare of inflammatory bowel disease as defined by Harvey-Bradshaw Index (HBI) \>6 (Crohn's disease) or Simple Clinical Colitis Activity Index (SCCAI) \>5 (ulcerative colitis). 5. Requiring a protein restricted diet as confirmed by a physician, for example chronic kidney disease stage 4 and 5 (estimated by Glomerular Filtration Rate \<30 mL/min/1.73 m2). 6. Requiring enteral nutrition (via tube delivery) or parenteral nutrition. 7. Subjects following a vegan diet.
Contact & Investigator
Danone Global Research & Innovation Center B.V.
✉ register.clinicalresearchnutricia@danone.com📞 +31 30 2095 000
Frequently Asked Questions
Who can join the NCT06781619 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Disease Related Malnutrition. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06781619 currently recruiting?
Yes, NCT06781619 is actively recruiting participants. Contact the research team at register.clinicalresearchnutricia@danone.com for enrollment information.
Where is the NCT06781619 trial being conducted?
This trial is being conducted at Mechelen, Belgium, Rotterdam, Netherlands.
Who is sponsoring the NCT06781619 clinical trial?
NCT06781619 is sponsored by Nutricia Research. The trial plans to enroll 80 participants.