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Labor Progress Indices and the Dynamics of the Individual Contraction During the Active Stage of Labor

NCT01009411 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2014-06-20

No results posted yet for this study

Summary

Objective of the study: to obtain new data on the dynamics of the labor process, cervix dilatation and head station on the labor process and to develop a new progress indices.

Background: the best method used today to supervise the labor process is to follow cervix dilatation and head station. Today, the physician or the midwife use manual examination to estimate cervix dilatation and head station. This examination is perform many times in a normal labor process, and even more if there is any delay. The information from these examinations is inaccurate and non-continuous. In case of delay in the labor process, the delay will diagnosed late, because the frequency of the manual examination is about once an hour.

With the assistance of the BirthTrack device we can get continuous data on the labor process and get indices to estimate the labor process progress without the use of vaginal (manual) examination.

40 women in an active labor will take part in the study.

Method: by connecting sensors to the woman abdomen, to the cervix and to the baby head we follow the cervix dilatation and the fetus head station.

Conditions

  • Labor

Sponsors & Collaborators

  • Barnev Ltd

    collaborator OTHER

  • Western Galilee Hospital-Nahariya

    lead OTHER_GOV

Principal Investigators

  • Prof. Ofer Barnea, Phd. · Barnev Ltd

  • Prof. Ofer Barnea, Phd. · Barnev Ltd

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-09-30
Primary Completion
2012-12-31
Completion
2012-12-31

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 NCT01009411 on ClinicalTrials.gov