Rambam health care campus
Haifa, Israel
NCT Number: NCT03944187
The study is conducted to assess several sonographic parameters for prediction of labor induction success. These parameters include cervical length, fetal head circumference, and fetal head to cervix angle.
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Notify Me18 year–45 year
Female
Observational
Haifa, Israel
Pregnant women at term over 37 weeks' gestation visiting the obstetric emergency room for various obstetric indications will be assessed. Women with obstetric or medical indication for induction will receive an explanation regarding the study protocol and will sign an informed consent.
After recruitment and during the evaluation in the obstetric emergency room, patients will undergo transvaginal sonography during which, cervical length, fetal head circumference and fetal head to cervix angle will be measured.
Relevant demographic and obstetric information will be collected from a computerized database.
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Transvaginal sonography for measurement of cervical length, fetal head circumference and fetal head to cervix angle .
Time frame: From admission to the obstetric emergency room up to 24 hours postpartum
Vaginal delivery rate after labor induction
Rambam Health Care Campus
Other
Sonographic Assessment of Fetal Head Circumference, Cervical Length and Fetal Head to Cervix Angle for Prediction of Labor Induction Success
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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