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临床试验/NCT03005080
NCT03005080已完成不适用

The Utility of Pharmacogenetic Testing in Managing Children With Persistent Gastroesophageal Reflux Disease Despite Therapy

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 51 人开始时间: 2016年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
51
试验地点
1
主要终点
Number of subjects who change medication due to pharmacogenomic results

研究概览

简要总结

This study will use a 22 gene pharmacogenomics panel on 30 children with persistent Gastroesophageal Reflux Disease (GERD) who have not responded to therapy.

详细描述

This study will assess the clinical utility of pharmacogenomics testing in the clinical management of children with refractory GERD, despite adequate therapy and the role of pharmacogenomics in selecting the right acid suppressive therapy based on each patient's symptoms and pharmacogenomics results.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
— 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

结局指标

主要结局

Number of subjects who change medication due to pharmacogenomic results

时间窗: 12 weeks

Number of subjects who have a repeat scope

时间窗: 12 weeks

次要结局

未报告次要终点

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Imad Absah

Imad Absah, M.D.

Mayo Clinic

研究点 (1)

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