Phase
Condition
N/ATreatment
budesonide
omeprazole (proton pump inhibitor)
Clinical Study ID
Ages 6-18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
CD diagnosed according to the commonly accepted Porto criteria, which take intoaccount clinical, endoscopic and histopathological criteria;
inflammatory changes in the esophagus and/or stomach and/or duodenum found in theendoscopic examination (assessed by 2 independent endoscopists) and confirmed in thehistopathological examination (in the Paris scale, CD activity: L4a, i.e.involvement of the upper gastrointestinal tract up to the ligament of Treitz);
stable, understood as no treatment modification, CD treatment for ≥2 weeks.
Exclusion
Exclusion Criteria:
other than CD, causes of inflammatory changes in the esophagus and/or stomach and/orduodenum such as: reflux esophagitis, herpetic esophagitis, cytomegalovirusesophagitis, eosinophilic esophagitis and/or gastritis and/or duodenitis,Helicobacter pylori infection;
use of systemic steroids for up to 30 days before enrollment in the study;
use of inhaled steroids for up to 30 days before enrollment in the study;
use of IPP for up to 30 days before enrollment in the study;
acute viral or bacterial infection for up to 30 days before enrollment in the study;
morning cortisol <5 ug/dl;
lack of informed consent from the child's parents or guardians to participate in thestudy; in the case of children ≥16 years of age, lack of the child's consent toparticipate in the study.
pregnancy
breastfeeding;
lack of consent of a woman of childbearing age or a fertile man to followcontraceptive recommendations during the study;
history of cancer in the patient.
Study Design
Study Description
Connect with a study center
Jagiellonian University
Kraków, 30-663
PolandSite Not Available
Poznań University of Medical Sciences
Poznań, 60-572
PolandSite Not Available
Medical University of Warsaw
Warsawa, 02-091
PolandSite Not Available
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