Pharmacogenetic Testing in Children With Persistent Gastroesophageal Reflux Disease (NCT03005080) | Clinical Trial Compass
CompletedNot Applicable
Pharmacogenetic Testing in Children With Persistent Gastroesophageal Reflux Disease
United States51 participantsStarted 2016-12
Plain-language summary
This study will use a 22 gene pharmacogenomics panel on 30 children with persistent Gastroesophageal Reflux Disease (GERD) who have not responded to therapy.
Who can participate
Age range18 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* persistent gastrointestinal symptoms (GI) suggestive of gastro esophageal reflux disease (GERD) despite adequate therapy
* persistent evidence of abnormal reflux indices' and acid exposure on esophageal multichannel pH impedance study despite adequate therapy
* persistent endoscopic evidence of reflux esophageal disease despite adequate therapy
Exclusion Criteria:
* children with eosinophilic esophagitis diagnosis
* children with any esophageal surgical intervention like fundoplication, tracheoespahgeal fistula repair or esophageal atresia repair
* children with other diseases that can affect the esophagus, like Crohn's disease or food protein-induced enterocolitis syndrome (F-PIES)
* Children who do not have research authorization in their chart
What they're measuring
1
Number of subjects who change medication due to pharmacogenomic results