Status:
UNKNOWN
Cervical Gland Area as a Predictor of Success of Labour Induction
Lead Sponsor:
Rambam Health Care Campus
Conditions:
Induced Vaginal Delivery
Eligibility:
FEMALE
18-45 years
Brief Summary
Women who fulfil the inclusion criteria and who are planned for labour induction will be recruited. Bishop score, cervical length, and the presence of cervical glandular area (CGA) will be documented ...
Detailed Description
Patient consent to participate in the study will be retrieved following the medical decision of labor induction and the mode of induction and following the patient consent to the induction. Bishop sc...
Eligibility Criteria
Inclusion
- Singleton and twins' pregnancies
- Pregnancy 34-41 weeks of gestation
- Vertex presentation
- Induction methods (Oxytocin, prostaglandin 1 (PGE1), prostaglandin 2 (PGE2), double balloon catheter, rupture of memebrane (ROM)
Exclusion
- Intrauterine fetal demise (IUFD)
- Contraindication to vaginal delivery
- Status post cervical cerclage
- Previous attempt of labor induction
- History of cervical surgery
- Active vaginal bleeding
Key Trial Info
Start Date :
June 7 2020
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
June 7 2022
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT04416022
Start Date
June 7 2020
End Date
June 7 2022
Last Update
June 4 2020
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