Intestinal fatty acid binding protein (I-FABP) as a promising test for Crohn's disease: a preliminary study.
Murat Sarikaya, Bilal Ergül, Zeynal Doğan...
https://pubmed.ncbi.nlm.nih.gov/25807642/Actively Recruiting
Led by Bursa City Hospital · Updated on 2026-06-24
100
Participants Needed
1
Research Sites
12 weeks
Total Duration
Researchers are studying children aged 2 to 18 years with IgA vasculitis to see if plasma intestinal fatty acid-binding protein I-FABP levels are linked to gastrointestinal problems. This observational study aims to find out if I-FABP can serve as a useful biomarker to detect gastrointestinal involvement in pediatric IgA vasculitis. The study enrolls children who meet specific classification criteria and follows them over time. During the study, blood samples are taken at diagnosis and again at a routine follow-up visit about 2 to 4 weeks later. Plasma from these samples will be used to measure I-FABP levels. Participants are grouped based on whether they have gastrointestinal symptoms or not. No experimental treatments or devices are given, as all procedures happen during standard care visits with the addition of blood sampling for research purposes. Participants provide clinical, laboratory, and demographic information at the start and follow-up visits. Researchers compare I-FABP levels and clinical data between groups to assess the association with gastrointestinal issues. The study monitors children through routine medical visits and collects data over a few weeks, aiming to identify noninvasive markers that can help detect gastrointestinal involvement early in IgA vasculitis.
CONDITIONS
I-FABP as a Predictor of Gastrointestinal Involvement in Pediatric IgA Vasculitis
N
Nur Şeyma Zengin, MD
T
Tuba Kurt, MD, Associate Professor
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Bursa City Hospital
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - At diagnosis
Participants provide blood samples and clinical data at diagnosis to measure plasma I-FABP levels and assess baseline health.
1 visit (in-person)
Duration - 2 to 4 weeks after diagnosis
Participants return for a routine follow-up visit 2 to 4 weeks after diagnosis for a second blood sample and clinical evaluation.
1 visit (in-person)
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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https://pubmed.ncbi.nlm.nih.gov/26798632/Bursa City Hospital
Lead Sponsor