Clinical Feasibility of Birth- Track II System

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00840710

Acronym

Enrollment

Registered

2009-02-10

Start date

2010-02-28

Completion date

2010-08-31

Last updated

2009-12-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Labor, Obstetrics

Keywords

women in active labor

Brief summary

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

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

FEMALE

Age

17 Years to 50 Years

Healthy volunteers

Yes

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)

Countries

Israel

Contacts

Primary ContactJacob Bornestein, Phd.

049107207

Outcome results