Clinical Feasibility of Birth- Track II System

NCT00840710 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 15

Last updated 2009-12-29

No results posted yet for this study

Summary

The Study purpose is to monitor the cervix dilation, head descent, FHR and to follow contraction in a women in active labor.

Conditions

  • Obstetrics
  • Labor

Sponsors & Collaborators

  • Barnev Ltd

    lead OTHER

Principal Investigators

  • Jacob Bornstein, PhD · Westren Gallilie Hospital

Eligibility

Min Age
17 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-02-28
Completion
2010-08-31

Countries

  • Israel

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 NCT00840710 on ClinicalTrials.gov