Clinical Feasibility of Birth- Track II System

Barnev Ltd15 enrolled

Overview

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

Study Type

OBSERVATIONAL

Enrollment

Conditions

Obstetrics Labor

Eligibility

Sex: FEMALEMin age: 17 YearsMax age: 50 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: 1. Laboring women referred to the Maternity Center in active labor (3cm dilatation and contractions). 2. Gestational age 37-42 weeks. (GA) 3. Single fetus 4. Subjects who understood, agreed and signed the informed consent form Exclusion Criteria: 1. Women with abnormal placentation (placenta previa) 2. Abnormal fetal presentation (breech presentation) 3. Maternal History of HIV and/or blood transmitted hepatitis and/or active genital Herpes. 4. Need for immediate delivery (cord prolapsed or suspected placental abruption)

Locations (1)

Westren Gallilie Hospital

Nahariya, Israel

Central Contacts

Jacob Bornestein, Phd.

CONTACT

049107207

Data from ClinicalTrials.gov

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