Crohn's Disease Clinical Trials

Find Crohn's Disease Clinical Trials Near You

Familial Inflammatory Bowel Disease Early Risk (Fiber) Study

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Brief Summary The aim of the FIBER study is to identify potential triggers associated with the later development of IBD (inflammatory bowel disease) based on baseline characteristics and biosamples (blood, urine, stool, saliva, and tissue). Aim 1: To identify clinical, demographic, and immunologic factors associated with an increased risk of developing IBD in family members of IBD patients. This aim will investigate the role of clinical factors (e.g., age of onset, gender, and family history), demographic factors (e.g., socioeconomic status, geographical location), and immune system markers (e.g., inflammatory cytokine profiles, immune cell populations) in predicting the likelihood of family members developing IBD over time. Aim 2: To examine dietary, environmental, and immunologic influences on the development of IBD in family members of IBD patients. This aim will explore how dietary habits (e.g., fiber, fats, processed foods), environmental exposures (e.g., smoking, pollution, and antibiotic use), and immune responses (e.g., changes in T-cell activation, inflammatory markers) contribute to the risk of IBD in family members. Aim 3: To analyze the multi-omic (metagenomic, transcriptomic, proteomic) cellular signatures of host and microbial signatures in family members of IBD patients and their association with IBD onset. This aim will investigate changes in the gut microbiome and immune-related gene expression profiles (transcriptomics) in family members. Specifically, the aim will focus on how shifts in microbial composition and host immune response genes (e.g., those involved in inflammation and epithelial barrier function) correlate with an increased risk of IBD development. Aim 4: To investigate the multi-omic (metabolomic, transcriptomic, proteomic) cellular signature of host and microbial signatures in family members to identify biomarkers predictive of IBD development. This aim will involve examining the metabolic, protein, and transcriptomic signatures (e.g., circulating cytokines, immune receptor expression) in blood, urine, or stool samples. The study will seek to identify early biomarkers from these profiles that can predict the onset of IBD, even in asymptomatic family members.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 55
Healthy Volunteers: t
View:

• Asymptomatic first degree relative (FDR) (siblings or offspring) of patients with CD or UC aged between 0 and 55 years.

Locations
United States
Washington
Seattle Children's Hospital
RECRUITING
Seattle
Contact Information
Primary
Cylia Abrous, BS
cylia.abrous@seattlechildrens.org
206-987-4701
Backup
Nuding Mason, Supervisor
mason.nuding@seattlechildrens.org
206-987-0055
Time Frame
Start Date: 2026-03-26
Estimated Completion Date: 2036-02
Participants
Target number of participants: 7000
Treatments
first-degree relatives of patients with CD or UC
Asymptomatic first degree relative (FDR) (siblings or offspring) of patients with CD aged between 0 and 55 years.~Exclusion criteria for each subject population:~* Nonviable neonates and uncertain viability neonates~* Antibiotic treatment within 3 months prior to recruitment~* Individuals with the presence of a known diagnosis of IBD, or symptoms suggestive of IBD~* Not within the age range of 0-55 years
Sponsors
Leads: Seattle Children's Hospital

This content was sourced from clinicaltrials.gov