Status:
UNKNOWN
Clinical Feasibility of Birth- Track II System
Lead Sponsor:
Barnev Ltd
Conditions:
Obstetrics
Labor
Eligibility:
FEMALE
17-50 years
Brief Summary
The Study purpose is to monitor the cervix dilation, head descent, FHR and to follow contraction in a women in active labor.
Eligibility Criteria
Inclusion
- Laboring women referred to the Maternity Center in active labor (3cm dilatation and contractions).
- Gestational age 37-42 weeks. (GA)
- Single fetus
- Subjects who understood, agreed and signed the informed consent form
Exclusion
- Women with abnormal placentation (placenta previa)
- Abnormal fetal presentation (breech presentation)
- Maternal History of HIV and/or blood transmitted hepatitis and/or active genital Herpes.
- Need for immediate delivery (cord prolapsed or suspected placental abruption)
Key Trial Info
Start Date :
February 1 2010
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
August 1 2010
Estimated Enrollment :
15 Patients enrolled
Trial Details
Trial ID
NCT00840710
Start Date
February 1 2010
End Date
August 1 2010
Last Update
December 29 2009
Active Locations (1)
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1
Westren Gallilie Hospital
Nahariya, Israel