Acceptability, Gastrointestinal Tolerance, Compliance and Palatability Study.
NCT ID: NCT07210658
Last Updated: 2026-01-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
25 participants
INTERVENTIONAL
2025-04-14
2026-05-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Children will act as their own control for the nutritional product
Oral nutritional supplementation
As directed by the HCP
Interventions
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Oral nutritional supplementation
As directed by the HCP
Eligibility Criteria
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Inclusion Criteria
* Patients well-established and stable on current nutritional support regimen.
* Willingly given, written, informed consent from patient/caregiver.
Exclusion Criteria
* Inability to comply with the study protocol, in the opinion of the investigator.
* Under 1 years of age
* Patients on total parenteral nutrition
* Known food allergies, including any allergies to the ingredients
* Patients with Chronic Kidney Disease (CKD) stage 3b (G3b), stage 4 (G4), stage 5 (G5) or hepatic impairment.
* Participation in another interventional study within 2 weeks of this study.
* Patients with known or suspected ileus or mechanical bowel obstruction
1 Year
16 Years
ALL
No
Sponsors
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Société des Produits Nestlé (SPN)
INDUSTRY
Responsible Party
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Locations
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Dietetics
Nottingham, , United Kingdom
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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ONS FB 001
Identifier Type: -
Identifier Source: org_study_id
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