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Evaluating the Safety of PregSense™ and Compare Its Performance to CTG in Prenatal Monitoring of Pregnant Subjects

Pregnancy Clinical Trial

Official title:
Clinical Study Evaluating the Safety of PregSense and Comparative Performance of PregSense Versus CTG in Prenatal Monitoring of Pregnant Subjects

Clinical Trial Summary

This clinical study will evaluate the safety of PregSense™ and Comparative Performance of PregSense™ versus CTG in Prenatal Monitoring of Pregnant subjects.

Clinical Trial Description

PregSense™ is a maternal-fetal monitor that non-invasively measures and displays fetal heart rate, maternal hear rate and uterine contractions. This study will be performed to collect and digitally record data from PregSense™ and the standard of care (CTG) in order to provide evidence of safety and agreement between PregSense™ and the gold standard NST device. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03504189
Study type Interventional
Source Nuvo-Group, Ltd.
Contact
Status Completed
Phase N/A
Start date March 1, 2018
Completion date November 8, 2018
View Details
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