Actively Recruiting

Age: 16Years +
All Genders
NCT06550310

Nutrition and Clinical Outcomes in IBD

Led by Barts & The London NHS Trust · Updated on 2026-02-19

300

Participants Needed

1

Research Sites

214 weeks

Total Duration

On this page

Sponsors

B

Barts & The London NHS Trust

Lead Sponsor

K

King's College London

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this observational study is to demonstrate that nutritional status and body composition have an impact on clinical outcomes in inflammatory bowel disease (IBD). The main objectives are: 1. To compare the detection rates of undernutrition between a range of nutritional screening tools, physiological measures and assessment tools amongst patients with different IBD phenotypes 2. To correlate nutritional status, nutritional biomarkers and body composition with clinical outcomes in patients with IBD treated with advanced medical therapy or surgery 3. To determine a potential relationship between radiological muscle mass measurements and clinical outcomes in patients with IBD treated with advanced medical therapy or surgery Participants will undergo an assessment at pre-treatment baseline and then again at their scheduled follow-up. This is a non-interventional study and participants will not be required to have any invasive tests or hospital visits beyond that of standard clinical care.

CONDITIONS

Official Title

Nutrition and Clinical Outcomes in IBD

Who Can Participate

Age: 16Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with inflammatory bowel disease (Crohn's disease, ulcerative colitis or IBD-U) starting a new advanced medical therapy
  • Patients with inflammatory bowel disease (Crohn's disease, ulcerative colitis or IBD-U) undergoing an IBD-related surgery
  • Age >16
  • Patients able and willing to provide written informed consent
Not Eligible

You will not qualify if you...

  • Patients below the age of 16
  • Patients who cannot provide informed consent
  • Patients with a cardiac pacemaker or internal defibrillator
  • Patients with active cancer and other disorders associated with severe cachexia

AI-Screening

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Trial Site Locations

Total: 1 location

1

Barts Health NHS Trust

London, United Kingdom, N15 4GL

Actively Recruiting

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Research Team

S

Sarah Faloon, MBChB

CONTACT

S

Shameer Mehta, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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