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Elemental 028 Extra Case Studies

Sponsor: Nutricia UK Ltd

NCT ID: NCT06877923

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Elemental 028 Extra (supplement)
How long the study runs
Study runs about 21 months (dates as stated)
About the drug or intervention
Elemental 028 Extra — supplement: Elemental 028 Extra formulations.
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
3 Years and over
Who
All
Number of participants
30
Started
2025-05-01
Last checked
2026-02

Plain English Summary

What is this study?

  • • Testing a new treatment for gastrointestinal disease
  • • NA - 30 participants
  • • Elemental 028 Extra is a nutritionally complete ACBS approved amino acid-based (elemental) feed designed to provide adequate daily amounts of both macronutrients and micronutrients when used as a sole source of nutrition and to support patients with severe impairment of the gastrointestinal tract who may require an elemental diet

Who can take part?

  • • Ages 3 Years and over
  • • Diagnosed with gastrointestinal disease

Where?

  • • Trowbridge - Nutricia UK

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

Elemental 028 Extra is a nutritionally complete ACBS approved amino acid-based (elemental) feed designed to provide adequate daily amounts of both macronutrients and micronutrients when used as a sole source of nutrition and to support patients with severe impairment of the gastrointestinal tract who may require an elemental diet. An upgraded formulation of Elemental 028 Extra with an increased energy, protein content micronutrient profile has been developed to better meet the nutritional requirements of patients. This series of case-studies aims to evaluate the acceptability, compliance, and gastrointestinal tolerance of the upgraded formulation of Elemental 028 Extra, in 30 adult and paediatric patients (15 powder and 15 liquid), with conditions where there is a severe impairment of the gastrointestinal tract, such as inflammatory bowel disease, short bowel syndrome, intractable malabsorption, allergic disease, and neurodegenerative diseases, and an elemental feed is required. The case study will last 29 days in total, including a 1-day baseline period followed by a 28-day intervention period. The case studies will be conducted across multiple centres in the UK, to meet the UK ACBS and GMS requirements for acceptability studies.

More detail

Medical nutrition feeds for the dietary management of gastrointestinal impairment and/or allergic diseases can be broadly classified into three categories according to the size of the protein source in the feed: polymeric, extensively or partially hydrolysed, and elemental feeds. Polymeric feeds contain whole protein sources, typically from milk, soy, or pea protein. Extensively or partially hydrolysed feeds, also referred to as oligopeptide or semi-elemental feeds, contain peptides which are on average 4-5 amino acids in length, and are typically hypoallergenic as the peptides are too short for antigen recognition or presentation. Elemental feeds, also referred to as amino acid-based, hydrolysed or pre-digested, contain single amino acids as a source of protein and have a broad clinical application amongst patients with conditions where there is a severe impairment of the gastrointestinal tract possibly due to maldigestion and/or malabsorption including inflammation, reduced concentration of digestive enzymes and/or reduced surface area for nutrient absorption associated with some diseases and treatments. Such conditions include gastrointestinal diseases or disorders, neuro-disabilities and neuro-degenerative diseases, gynaecological cancers, and gastrointestinal impairment secondary to clinical treatment. Allergic diseases can also be managed with elemental feeds. Elemental 028 Extra is a nutritionally complete ACBS approved amino acid-based (elemental) feed designed to provide adequate daily amounts of both macronutrients and micronutrients when used as a sole source of nutrition and to support patients with severe impairment of the gastrointestinal tract who may require an elemental diet. An upgraded formulation of Elemental 028 Extra with an increased energy, protein content and micronutrient profile has been developed to better meet the nutritional requirements of patients. This series of case-studies aims to evaluate the acceptability, compliance, and gastrointestinal tolerance of the upgraded formulation of Elemental 028 Extra, in 30 adult and paediatric patients (15 powder and 15 liquid), with conditions where there is a severe impairment of the gastrointestinal tract, such as inflammatory bowel disease, short bowel syndrome, intractable malabsorption, allergic disease, and neurodegenerative diseases, and an elemental feed is required. The case study will last 29 days in total, including a 1-day baseline period followed by a 28-day intervention period. The case studies will be conducted across multiple centres in the UK, to meet the UK ACBS and GMS requirements for acceptability studies.

Gastrointestinal DiseaseInflammatory Bowel Disease (IBD)Short BowelMalabsorptionAllergiesNeurodegenerative Disorders

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 3 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Male or female
  • ✓Over 3 years of age
  • ✓Requiring an elemental feed (at least 30% of total energy requirements)
  • ✓Written or electronic agreement to take part from patient, and/or from parent/caregiver if applicable

Who cannot take part

  • ✗Pregnant or lactating
  • ✗Requiring parenteral nutrition
  • ✗Major liver or kidney dysfunction
  • ✗Participation in other studies within 1 month prior to entry of this study
  • ✗Investigator concern around willingness/ability of patient or parent/caregiver to comply with protocol requirements
See the full criteria
Inclusion Criteria: * Male or female * Over 3 years of age * Requiring an elemental feed (at least 30% of total energy requirements) * Written or electronic informed consent from patient, and/or from parent/caregiver if applicable Exclusion Criteria: * Pregnant or lactating * Requiring parenteral nutrition * Major hepatic or renal dysfunction * Participation in other studies within 1 month prior to entry of this study * Investigator concern around willingness/ability of patient or parent/caregiver to comply with protocol requirements

Where Is This Study? (1 UK site)

Nutricia UK

Trowbridge, United Kingdom

Recruiting
Site contact (verified)

How to Get in Touch

Isabel Evans

Sponsor contact

CONTACT

+44 7385 000738 isabel.evans@nutricia.com
Data sourced from ClinicalTrials.gov · Last verified: 2026-02