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Clinical Trial Summary

The investigators will compare the effectiveness of gabapentin to metoclopramide for 1 week among 60 women with hyperemesis gravidarum (HG) in this randomized, double-blinded trial. After completion of the 1-week double-blind phase, subjects will be offered open-label gabapentin with rescue metoclopramide until their symptoms no longer require treatment. Enrollment will occur at the University's at Buffalo, of Rochester and of Wisconsin.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02163434
Study type Interventional
Source State University of New York at Buffalo
Contact
Status Completed
Phase Phase 2
Start date June 2014
Completion date November 2019

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