Hemorrhagic Proctocolitis Clinical Trials

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Impact of Diet on the Effectiveness of Anti-TNF Therapy in Inflammatory Bowel Disease: a Prospective, Randomized, Double Arm, Open-label Study

Status: Recruiting
Location: See location...
Intervention Type: Combination product, Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Participant is willing and able to give informed consent forparticipation in the study

• Males or Females, Adults aged 18 years or older

• Confirmed diagnosis of moderate-to-severe Crohn's disease orulcerative colitis

• Patients who are planned to start anti-TNF therapy

• Ability and willingness to comply with the Crohn's DiseaseExclusion Diet (CDED)

Locations
Other Locations
Italy
IRCCS Ospedale San Raffaele
RECRUITING
Milan
Contact Information
Primary
Tommaso Lorenzo Parigi, MD
parigi.tommaso@hsr.it
+39 02 2643 2756
Backup
Annunziata Bruno, MS
bruno.annunziata@hsr.it
+39 02 2643 2756
Time Frame
Start Date: 2025-05-22
Estimated Completion Date: 2027-10-01
Participants
Target number of participants: 80
Treatments
Experimental: Intervention group
Patients who accept participation and are randomized to receive dietary advice on the CDED diet will be included in the intervention group.
Active_comparator: Control group
The control group will receive only anti-TNF therapy as per the standard of care and guidelines recommendation
Sponsors
Leads: IRCCS Ospedale San Raffaele

This content was sourced from clinicaltrials.gov