Clinical Feasibility of Birth- Track II System (BT)

Barnev

Status: Unknown

Conditions: Labor; Obstetrics

Study type: Observational

Funder types: Other

Identifiers

NCT00840710

BT-II-IS-001

Details and patient eligibility

About

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

Enrollment: 15 estimated patients

Sex: Female

Ages: 17 to 50 years old

Volunteers: Accepts Healthy Volunteers

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)