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Biologics and Paediatric Enteral Nutrition in Crohn's Disease Study (BIOPIC-Kids): Combining Enteral Nutrition With Biologics to Optimise Induction and Maintenance Therapy for Children With Active Crohn's Disease

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Crohn's disease (CD) is a chronic, incurable condition associated with gut inflammation. Two important treatments currently used to manage CD are special drug injections (biologics) or a liquid-only diet using specialised milkshakes. However, treatment with biologics is only successful in approximately 55-60%. The liquid-only diet also has a better safety and effectiveness profile than traditional treatments like steroids. However, gut inflammation often returns not long after the normal diet is re-introduced, and it is difficult for patients to stick to as their sole source of nutrition for 6-8 weeks. The BIOPIC-Kids study aims to investigate whether replacing the normal diet with specialised milkshakes for 6 weeks improves response to treatment and maintenance of remission with biologics in children and young adults with CD. To achieve this, children and young adults (aged 6-18 years) with active CD commencing biologics as standard of care treatment will be randomly allocated to follow their normal diet OR replace varying amounts of their normal diet with specialised milkshakes for 6 weeks. Participants not wanting to be randomised can choose the group of their preference. Patients starting a liquid-only diet OR biologics alongside a liquid-only diet as standard of care treatment will also be recruited to compare different treatment outcomes.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 6
Maximum Age: 18
Healthy Volunteers: t
View:

• Eligible participants to the RCT are children or young adults (aged 6 to 18 years old) who have active CD (defined as a weighted paediatric Crohn's disease Activity Index score (wPCDAI) ≥ 12.5 or a Faecal Calprotectin level \>250 mg/kg and who have a clinical indication to initiate standard of care induction treatment with TNFα inhibitors (infliximab or adalimumab).

• Eligible participants to the observational cohorts are children or young adults (aged 6 to 18 years old) who have active CD (defined as a weighted paediatric Crohn's disease Activity Index score (wPCDAI) ≥ 12.5 or a Faecal Calprotectin level \>250 mg/kg and who are due to initiate standard of care induction treatment with EEN therapy alongside TNFα inhibitors (infliximab or adalimumab) or standard of care induction treatment with EEN therapy without TNFα inhibitors (infliximab or adalimumab)

Locations
Other Locations
United Kingdom
The Royal Aberdeen Children's Hospital
NOT_YET_RECRUITING
Aberdeen
University Hospital Crosshouse
NOT_YET_RECRUITING
Crosshouse
Ninewells Hospital
NOT_YET_RECRUITING
Dundee
Royal Hospital for Children & Young People
RECRUITING
Edinburgh
Royal Hospital For Children
RECRUITING
Glasgow
University Hospital Wishaw
NOT_YET_RECRUITING
Wishaw
Contact Information
Primary
Konstantinos Gerasimidis, Professor
Konstantinos.Gerasimidis@glasgow.ac.uk
+441419560580
Backup
Sophie F Morris, BSc (Hons)
s.morris.2@research.gla.ac.uk
+447887804802
Time Frame
Start Date: 2026-03-27
Estimated Completion Date: 2030-08
Participants
Target number of participants: 90
Treatments
Experimental: Enteral Nutrition
Paediatric patients allocated to the enteral nutrition study arm will be asked to replace varying amounts of their daily energy requirements with a proprietary formula (Ready-To-Drink Modulen, Nestle, or Modulen IBD, Nestle) for 6 weeks alongside standard of care treatment with infliximab or adalimumab as induction therapy.
No_intervention: Unrestricted Diet
Paediatric patients allocated to the unrestricted diet study arm will be asked to follow their habitual, unrestricted diet for 6 weeks alongside standard of care treatment with infliximab or adalimumab as induction therapy.
No_intervention: Exclusive Enteral Nutrition
An observational cohort of paediatric patients receiving standard of care treatment with exclusive enteral nutrition as induction therapy.
No_intervention: Exclusive enteral nutrition alongside Infliximab or Adalimumab Induction Therapy
An observational cohort of paediatric patients receiving standard of care treatment with exclusive enteral nutrition alongside infliximab or adalimumab as induction therapy.
Related Therapeutic Areas
Sponsors
Collaborators: NHS Grampian, NHS Lanarkshire, NHS Ayrshire and Arran, NHS Lothian, NHS Tayside, NHS Greater Clyde and Glasgow
Leads: University of Glasgow

This content was sourced from clinicaltrials.gov