Ahmed Abbas
Assiut, Cairo Governorate, 002, Egypt
NCT Number: NCT04325256
Induction of labour (IOL) nowadays is a common procedure in obstetric practice. Presently, IOL is done for 20% of pregnancies for various maternal and fetal indications and nearly 20% of labour inductions end up in caesarean deliveries. The success of IOL mainly depends upon "favourability" of the cervix which is usually assessed by manual examination and Scored as Bishop Score. However, this method is limited by subjectivity and reproducibility and though done in all the patients prior to IOL, several studies have demonstrated poor correlation between Bishop Score and outcome of IOL
Looking for future studies?
Notify MeFemale
Observational
Assiut, Cairo Governorate, 002, Egypt
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
length of the cervix from the internal to external os, presence or absence of funneling and if present width and length of funneling at internal os were measured. Distance between presenting part to external os will be measured and position of the cervix i.e. whether curved or straight will also noted.
maternal height, parity, body-mass index (BMI) at delivery and the results of modified Bishop's score in calculation of probability of CS
Time frame: 24 hours
an ability to achieve the active phase of labor corresponding to a cervical dilatation of ≥4 cm within 12 h of initiating oxytocin on the first day of induction
Assiut University
Other
Accuracy of Different Scoring Systems for Predicting Successful Induction of Labor: a Cross-sectional Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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.
Published trials that share one or more normalized conditions with this study.
NCT04478942
Female Urogenital Diseases and Pregnancy Complications, Fetal Membranes, Premature Rupture
Madison, Wisconsin, United States
View Trial DetailsNCT02975167
Behavior, Cervical Ripening
Long Beach, California, United States
View Trial DetailsNCT06122168
Induction of Labor Affected Fetus / Newborn, Nulliparity
Ponderano, Biella, Italy
View Trial DetailsNCT03544606
Induction of Labor Affected Fetus / Newborn
Kafr ash Shaykh, Egypt
View Trial Details