Gastrointestinal Dysmotility on Aspiration Risk

Status Not yet recruiting

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

Clinical Trial Details

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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