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Clinical Trial Summary

The hypothesis of this study is that esophageal and gastric dysmotility increase the risk of developing aspiration-associated symptoms in children with neurologic impairment. The investigators are conducting a ten week cross over study comparing prucalopride to famotidine for the treatment of aspiration-associated symptoms.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05455359
Study type Interventional
Source Boston Children's Hospital
Contact Rachel Rosen, MD
Phone 617-355-0897
Email rachel.rosen@childrens.harvard.edu
Status Not yet recruiting
Phase Phase 4
Start date July 18, 2022
Completion date July 18, 2027

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