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Clinical Trial Summary

The aim of the study is to evaluate the efficacy of the stimulant laxative Senokot-S® for the treatment of diabetic gastroparesis. Senokot-S, and its metabolites, are thought to produce peristalsis, drive intraluminal fluid and electrolyte shifts, and have an irritant effect on the gut mucosa. These complex physiologic mechanisms appear may sufficiently promote stomach emp-tying, and thereby reduce or eliminate the severity of gastroparesis symptoms. In this open label study, participants will be randomized into high and low dose groups to assess for ideal dosing and tolerability. It is the overall goal of this study to select the most promising dose-strength for the treatment of mild through severe gastroparesis.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03342157
Study type Interventional
Source Aurora Health Care
Contact
Status Terminated
Phase Phase 2
Start date April 2, 2018
Completion date August 17, 2018

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