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Clinical Trial Summary

The purpose of this study is to compare the feasibility and accuracy of two methods of non-invasive hemodynamic assessments - bioreactance as assessed by non-invasive cardiac output monitoring (NICOM; Cheetah Medical) and pulse wave analysis as assessed by finger cuff arterial pressure (ClearSite, Edwards Life Sciences) - compared to hemodynamic assessments by intermittent echocardiography in early onset preeclampsia.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05299229
Study type Observational
Source Yale University
Contact
Status Completed
Phase
Start date December 29, 2020
Completion date December 31, 2021

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