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Study to Support Fetal Heart Rate and Uterine Contraction for Preterm Labor in Singleton and Multiple Pregnancies

NCT01360905 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 8

Last updated 2014-01-20

No results posted yet for this study

Summary

The purpose of this study is to compare the Monica AN24 fetal monitor to previously FDA approved devices for Fetal Heart Rate and Uterine Contractions in labor for Multiples and pre term labor.

Conditions

  • Pre Term Labor
  • Multiple Pregnancy

Sponsors & Collaborators

  • New York Presbyterian Hospital

    collaborator OTHER

  • Monica Healthcare Ltd

    lead INDUSTRY

Principal Investigators

  • Fadi Mizra, Dr · New York Presbytarian Hospital

Eligibility

Min Age
17 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2012-07-31
Completion
2014-01-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01360905 on ClinicalTrials.gov