bioespecimen samples
ProcedureBlood, serum, plasma, urine, stools, small/large bowel tissue.
NCT Number: NCT05698745
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).
Interested in participating?
Request Info18 year and older
All sexes
Observational
Hospital Clínico Universitario de Santiago, Santiago de Compostela, A Coruña, Spain
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).
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:
Patients from cohort B will be included if they fulfill all the following inclusion criteria:
Patients from cohort C will be included if they fulfill all the following inclusion criteria:
Exclusion criteria
Patients from cohort A will be excluded if they fulfill any the following exclusion criteria:
Patients from cohort B will be excluded if they fulfill any the following exclusion criteria:
Patients from cohort C will be excluded if they fulfill any the following exclusion criteria:
Blood, serum, plasma, urine, stools, small/large bowel tissue.
Time frame: 10 years
Development and type of new-onset symptoms during follow-up (mainly diarrhea, abdominal pain, and rectal bleeding).
Time frame: 10 years
Time to development of symptomatic disease during follow-up.
Time frame: 10 years
Time frame: 10 years
proteomic, transcriptomic, serologic, microbiota, and tissue data
Time frame: 10 years
Time frame: 10 years
Time frame: 10 years
Time frame: 10years
Time frame: 10years
Time frame: 10years
Time frame: 10years
Contact information is provided by the study sponsor or research team.
Erika Araya, PhD
CONTACT
Iago Rodriguez Lago, MD
CONTACT
Grupo Espanol de Trabajo en Enfermedad de Crohn y Colitis Ulcerosa
Other
Prospective Study of the Natural History, Immunological and Genetic Characteristics of Preclinical Inflammatory Bowel Disease
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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