Condition: Eosinophilic Esophagitis · Sponsor: University of Colorado, Denver
The goal of this clinical trial is to \[primary purpose: e.g., learn if intervention or health behavior can treat, prevent, diagnose etc.\] in \[describe participant population/primary condition; could include any of the following: sex/gender, age groups, healthy volunteers\]. The main question\[s\] it aims to answer \[is/are\]: Does dupilumab or swallowed topical fluticasone improve the diameter of the esophagus more? Does dupilumab or swallowed topical fluticasone reduce inflammation in the esophagus more? Are comparative effective clinical trials feasible in this patient population? Researchers will compare dupilumab 300 mg weekly compared to swallowed fluticasone to see if there is a difference in treatment response. Participants will be asked to: * Be randomized to either dupilumab sq weekly or swallowed topical fluticasone twice daily. * Participate in 8 study visits over 52 weeks * Complete questionnaires * Have an endoscopy with biopsies and EndoFLIP measurements. * Swallow an Esophageal String Test
This description comes directly from the study's public registry record.
Michelle Landis, BS · 720-777-8884 · michelle.landis@childrenscolorado.org
Always discuss trial participation with your own doctor first.
| Children's Hospital Colorado/University of Colorado School of Medicine | Aurora, Colorado, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06705387