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Clinical Trial Summary

This is a single site pilot randomized, controlled, trial randomizing patients with PE with severe features to one of 2 groups: - 24 hours of postpartum magnesium sulfate (current arbitrary standard of care) - Using the Cheetah® device to aid in an individualized duration of magnesium sulfate.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04474704
Study type Interventional
Source Ohio State University
Contact
Status Completed
Phase N/A
Start date February 22, 2021
Completion date May 31, 2022

See also
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