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Accuracy and Reliability of Fetal Heart Rate and Uterine Contraction Monitoring Method | Clinical Trials | Clareo Health

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COMPLETEDNANCT01280357

Accuracy and Reliability of Fetal Heart Rate and Uterine Contraction Monitoring Method

Clinical Investigation Protocol for a study designed to determine the equivalence of the Monica AN24 monitor to Philips 50XM for fetal heart rate (FHR) and uterine contraction (UC) monitoring during l...

Lead sponsor: Monica Healthcare Ltd•2 U.S. locations•View source on ClinicalTrials.gov

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Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment60

Start dateFeb 2010

Last updatedMar 21, 2013

Condition

Pregnancy; Habitual Aborter Weeks of Gestation 37 or More

Locations shown

Queens Hospital Center

New York, New York

Temple University

Philadelphia, Pennsylvania

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: March 21, 2013Data synced to Clareo: July 13, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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