Image

Impact of Exclusion Diet in Addition to Anti-TNF Therapy in Crohn's Disease and Ulcerative Colitis: a Prospective, Randomized, Double-arm, Open-label Study

Impact of Exclusion Diet in Addition to Anti-TNF Therapy in Crohn's Disease and Ulcerative Colitis: a Prospective, Randomized, Double-arm, Open-label Study

Recruiting
18 years and older
All
Phase N/A

Powered by AI

Overview

This clinical study protocol aims to prospectively compare the efficacy of standard therapy with anti-TNF agents combined with the Crohn's Disease Exclusion Diet (CDED) versus anti-TNF therapy alone in adult patients with active Crohn's disease or ulcerative colitis.

The study will involve patients starting therapy with anti-TNF agents due to active Crohn's disease or ulcerative colitis as per standard clinical practice and in accordance with European (ECCO) guidelines.

One group will receive standard medical therapy only, the other will additionally receive dietary advice on how to adhere on a specific exclusion diet, the CDED.

By prospectively evaluating the impact of this combined approach, the study seeks to provide evidence on whether CDED can improve response to treatment and therefore improve quality of life for patients with Crohn's disease and ulcerative colitis.

Description

This is a prospective interventional, single-center, double-group, open-label study.

Primary objective is to compare the efficacy of CDED in addition to anti-TNF therapy in active CD and UC versus anti-TNF therapy alone.

Secondary objective are:

  • Endoscopic response
  • Endoscopic remission
  • Early and late efficacy and persistence of benefits
  • Biochemical response
  • Sonographic improvement
  • Tolerability and compliance to the Crohn's Disease ExclusionDiet (CDED)
  • Quality of life-Safety of the combination of biological therapy and CDED. The subjects considered are adult patients diagnosed with moderate-to-severe Crohn's disease or moderate-to-severe ulcerative colitis who are starting therapy with an approved anti-TNF agent (infliximab and adalimumab for both UC and CD, and golimumab only for UC).

Eligibility

Inclusion Criteria:

  1. Participant is willing and able to give informed consent forparticipation in the study
  2. Males or Females, Adults aged 18 years or older
  3. Confirmed diagnosis of moderate-to-severe Crohn's disease orulcerative colitis
  4. Patients who are planned to start anti-TNF therapy
  5. Ability and willingness to comply with the Crohn's DiseaseExclusion Diet (CDED)

Exclusion Criteria:

  1. Patients with undetermined inflammatory bowel disease
  2. Patients with metabolic or gastrointestinal conditions that couldinterfere or are incompatible with the study intervention (e.i.celiac disease, diabetes etc)
  3. Patients with a body-mass index lower than 17 or greater than30
  4. Patients who previously underwent intestinal resectionirrespective of cause
  5. Patients currently on exclusive enteral nutrition (EEN)
  6. Patients who have previously used or are currently adhering toCDED
  7. Pregnant or breastfeeding women
  8. Patients with a history of severe allergic reactions orintolerance to any food recommended in CDED
  9. Patients with significant comorbidities that may interfere withthe study or pose a risk to the participant
  10. Inability or unwillingness to comply with study protocols orfollow-up schedules

Study details
    Ulcerative Colitis (UC)
    Crohn Disease (CD)

NCT06896305

IRCCS Ospedale San Raffaele

1 February 2026

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.