NCT07522528 Biologics and Paediatric Enteral Nutrition in Crohn's Disease Study
| NCT ID | NCT07522528 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University of Glasgow |
| Condition | Crohn's Disease (CD) |
| Study Type | INTERVENTIONAL |
| Enrollment | 90 participants |
| Start Date | 2026-03-27 |
| Primary Completion | 2030-08 |
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 90 participants in total. It began in 2026-03-27 with a primary completion date of 2030-08.
⚠ 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
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 Criteria
Inclusion Criteria: * 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) Exclusion Criteria: * Inability to provide consent to participate in the study (i.e., this applies to young adults (aged 16-18 years) who are old enough but unable to provide consent and carers (of children aged 6-15 years old) who are unable to provide consent on behalf of their child). * Presence of stoma or of short bowel syndrome. * Patients currently receiving oral or intravenous steroids at a dosage \>20mg/day prednisolone or \>9mg/day budesonide. * Patients who start another induction therapy (e.g., high dosage of steroids) or change the dose of background immunomodulator (azathioprine, mercaptopurine, methotrexate) within the past 4 weeks. * CD with a major fistulising or symptomatic fibrotic stricturing phenotype. * Patients with comorbid anorexia nervosa. * Any clinical contraindication to use of exclusive enteral nutrition or partial enteral nutrition. * Patients tested positive for blood-borne viruses such as HIV and Hepatitis B and C. * Patients with untreated tuberculosis (latent or active). * Current enrolment in other studies of an investigational product or dietary intervention. * Food allergies, which do not permit participation in the study (e.g., cow's milk allergy). * Pregnant and/or breastfeeding individuals.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07522528 clinical trial?
This trial is open to participants of all sexes, aged 6 Years or older, up to 18 Years, studying Crohn's Disease (CD). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07522528 currently recruiting?
Yes, NCT07522528 is actively recruiting participants. Contact the research team at Konstantinos.Gerasimidis@glasgow.ac.uk for enrollment information.
Where is the NCT07522528 trial being conducted?
This trial is being conducted at Aberdeen, United Kingdom, Crosshouse, United Kingdom, Dundee, United Kingdom, Edinburgh, United Kingdom and 2 additional locations.
Who is sponsoring the NCT07522528 clinical trial?
NCT07522528 is sponsored by University of Glasgow. The trial plans to enroll 90 participants.
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