Cervical Gland Area as a Predictor of Success of Labour Induction

Induced Vaginal Delivery Clinical Trial

Official title: Cervical Gland Area as a Predictor of Success of Labour Induction

Status Not yet recruiting

Clinical Trial 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 for every patient up to 12 hours prior to the induction process, and patient information and maternal and neonatal outcome will be documented following the delivery.

Clinical Trial 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 score, cervical length, and the presence of cervical glandular area (CGA) will be documented for every patient up to 12 hours prior to the induction process.

The method of induction, data regarding patient demographics, the progress of labor, and the maternal and neonatal outcome will be documented following the delivery. ;

Related Conditions & MeSH terms

• Induced Vaginal Delivery

• NCT number: NCT04416022
• Study type: Observational
• Source: Rambam Health Care Campus
• Contact: Saar Aharoni, M.D
• Phone: + 523395351
• Email: s_aharoni@rambam.health.gov.il
• Status: Not yet recruiting
• Start date: June 7, 2020
• Completion date: June 7, 2022