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NCT Number: NCT05698745

Immunological Characteristics of Preclinical IBD

The purpose of this study is to evaluate disease progression, in terms of development of symptomatic disease and complications associated with IBD (e.g. fistula, abscess, stricture).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hospital Clínico Universitario de Santiago, Santiago de Compostela, A Coruña, Spain

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About this study

This is a prospective, observational, multicenter, collaborative research project that will explore the earlier stages of IBD, before the onset of the first symptoms of the disease. This novel approach constitutes an innovative strategy on the research on the natural history of the disease. The study will be carried out based on colorectal cancer screening colonoscopies, recruiting all patients with a new diagnosis of IBD in this setting. These patients will undergo follow-up visits every 6 months for 10 years and the clinical information will be enriched with longitudinal multi-omic analyses.

Two additional control groups will be identified, including patients with new-onset symptomatic IBD in the last 3 months and healthy controls (with normal screening colonoscopy).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patients from cohort A will be included if they fulfill all the following inclusion criteria:

  • Male or female ≥18 years of age at baseline.
  • New diagnosis of IBD during a CRC screening colonoscopy, based on the criteria from the European Crohn's and Colitis Organization (33, 34).
  • Presence of a chronic inflammatory infiltrate and histological diagnosis compatible with IBD.
  • The patient must be asymptomatic at diagnosis and without previous symptoms suggestive of IBD.
  • Time interval between the index colonoscopy and the baseline visit up to 3 months.

Patients from cohort B will be included if they fulfill all the following inclusion criteria:

  • Male or female ≥18 years of age at baseline.
  • Recent diagnosis of IBD, with <3 months from symptoms onset.
  • Time interval between the index colonoscopy and the baseline visit up to 3 months.

Patients from cohort C will be included if they fulfill all the following inclusion criteria:

  • Male or female ≥18 years of age at baseline.
  • No endoscopic signs of IBD after a complete ileo-colonoscopy within the CRC screening program.
  • Time interval between the index colonoscopy and the baseline visit up to 3 months.

Exclusion criteria

Patients from cohort A will be excluded if they fulfill any the following exclusion criteria:

  • Identification of any enteropathogen in the stool culture.
  • Isolated findings of acute inflammatory infiltrate without signs of chronicity.
  • Previous or current diagnosis of microscopic colitis.
  • Alteration in biomarkers in blood or stool will not constitute an exclusion criterion.

Patients from cohort B will be excluded if they fulfill any the following exclusion criteria:

  • Previous use of immunomodulators or biologics for any condition.

Patients from cohort C will be excluded if they fulfill any the following exclusion criteria:

  • Any gastrointestinal symptoms at baseline.
  • Previous use of immunomodulators or biologics for any condition.

Treatment and study plan

bioespecimen samples

Procedure

Blood, serum, plasma, urine, stools, small/large bowel tissue.

Primary outcomes

  1. Disease progression

    Time frame: 10 years

    Development and type of new-onset symptoms during follow-up (mainly diarrhea, abdominal pain, and rectal bleeding).

  2. Disease progression

    Time frame: 10 years

    Time to development of symptomatic disease during follow-up.

  3. - IBD characteristics

    Time frame: 10 years

    • Type (CD or UC)
    • Disease extent (CD or UC) according to Montreal classification
    • CD phenotype at diagnosis (Montreal classification)
    • Endoscopic characteristics at diagnosis (both CD and UC): type of lesions, distribution, and extent
    • Presence and type (simple, complex fistula or abscess) of perianal disease at diagnosis and during follow-up
  4. Omic findings

    Time frame: 10 years

    proteomic, transcriptomic, serologic, microbiota, and tissue data

Secondary outcomes

  1. IBD characteristics:

    Time frame: 10 years

    • Development and time to development of changes in CD disease location, according to Montreal classification.
    • Development and time to development of new-onset or stricturing, penetrating or perianal complications, defined as changes in CD phenotype (Montreal classification)
    • Development of proximal disease extension in UC
    • Laboratory parameters: FOBT levels at diagnosis, and CRP, hemoglobin, albumin, fecal calprotectin at diagnosis and during follow-up.
  2. Changes in endoscopic features during follow-up

    Time frame: 10 years

  3. Microscopic characteristics at diagnosis

    Time frame: 10 years

  4. Clinical disease activity during follow-up

    Time frame: 10years

  5. Development and time to development of need for medical or surgical therapy during follow-up

    Time frame: 10years

  6. Development and time to development of extraintestinal manifestations during follow-up

    Time frame: 10years

  7. Type of extraintestinal manifestations during follow-up

    Time frame: 10years

Study contacts

Contact information is provided by the study sponsor or research team.

Erika Araya, PhD

CONTACT

[email protected]

+34 674682070

Iago Rodriguez Lago, MD

CONTACT

[email protected]

+34 674682070

Sponsors and collaborators

Lead sponsor

Grupo Espanol de Trabajo en Enfermedad de Crohn y Colitis Ulcerosa

Other

Registry information

Official study title

Prospective Study of the Natural History, Immunological and Genetic Characteristics of Preclinical Inflammatory Bowel Disease

Important dates

Study start
2024
Primary completion
2026
Study completion
2038
First posted
Jan 26, 2023
Registry last updated
Apr 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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