Clinical Trials Logo

Clinical Trial Summary

Induction of labor is a widely used intervention in OBGYN practice. Doctors still use the old Bishop score in patients' follow up. It remains difficult to anticipate the outcomes and the possibility of adverse effects during this process. In this large prospective multicentric interventional study, we aim to develop a more precise and sensitive score based on machine learning tools programmed on python 3.8

This new tool will account for many variables in patient demography(age, race, weight ... etc ) and medical history (previous OBGYN surgery, comorbidities .... etc). These variables not usually found in the classic bishop score. We predict that our analysis will aid doctors in making better decisions and efficiently predict the outcomes, need for switching to operative delivery and possible complications.

Machine learning and digital calculation of hazards will allow more precise assessment and more efficient management during IOL as it considers variables not included in clinical scores.

this study aims to provide modern and efficient assessment parameters to guide clinical decision making during the IOL process and help doctors predict its outcomes based on subtle factors not usually considered.

This will minimize the complications and allow more evidence-based practice.


Clinical Trial Description

the objective is to create a database registry documenting the induction of labor (IOL) process and apply machine learning tools to create a more precise assessment score for doctors as a contemporary follow-up method.

we will collect data from at least 12 centers worldwide describing the course, outcomes, maternal or fetal complications, and any related data. The data will be collected after ethical approval and from consenting patients in a prospective manner. during the period from July 1st, 2020 to June 30th, 2021 (anticipated dates).

each center will be responsible for quality assessment, data collection, and ensuring the data is accurate, complete, and representative.

Data collection includes baseline pelvic examination (cervical position, consistency, dilation, effacement, fetal position, and bishop score), method of induction and their time of administration in relation to index time (start of IOL), findings and time of serial pelvic examinations, fetal heart tone, and maternal vital signs. The entry of data from serial examinations will continue during active labor and fetal and maternal outcomes will be reported. If the diagnosis of failed IOL is made and obstetric team decides delivery by Cesarean section, criteria of diagnosis/indication of Cesarean delivery will be reported. Length of active labor and the second stage will be documented, and maternal/perinatal complications will be reported. the collectors must ensure patient confidentiality and safety.

Inclusion criteria:-

- Pregnant women admitted for IOL, aged between 18 to 40 years

- Term or late preterm pregnancy (gestational age at 34 weeks or beyond)

- A reassuring fetal heart tracing prior to IOL

Exclusion criteria:-

- Fetal growth restriction with abnormal Doppler indices

- Intrauterine fetal death

- Suspected intra-amniotic infection prior to IOL

- Fetal major congenital anomalies

- Patients who decline IOL in prior or during IOL without medical indication

statistical analysis :- Data will be described using (mean, median, standard deviation, range) in the final sample. Machine learning method is superior to traditional statistical methods as it provides robust and automatic estimation of complex relationships between different variables and clinical outcomes. Data will be utilized as xi and yi where xi presents input (features) and yi presents dependent variables (outcomes). Functional regression is based on support vector machine by regressing the outcomes yi on inputs xi. Model Validation will be performed via bootstrap estimation to evaluate the predictive ability of the functional regression models. Data will be split to training data (approximately 63% of the data) to create prediction model where bootstrapping will be applied, and testing data where prediction model will be validated. Machine learning models will be created using python 3.8. ;


Study Design


Related Conditions & MeSH terms

  • Induction of Labor Affected Fetus / Newborn

NCT number NCT04350437
Study type Interventional
Source Assiut University
Contact Sherif A shazly, M.S
Phone +15075131392
Email sherif.shazly.mogge@gmail.com
Status Not yet recruiting
Phase N/A
Start date July 1, 2020
Completion date July 30, 2021

See also
  Status Clinical Trial Phase
Recruiting NCT04492150 - Effect of Glucose 5% on Labor Length N/A
Not yet recruiting NCT03625518 - Mode of Induction in Fetal Growth Restriction and Its Affects on Fetal and Maternal Outcomes Early Phase 1
Completed NCT04496908 - Early Versus Delayed Artificial Rupture of Membranes (AROM Trial) Early Phase 1
Recruiting NCT04478942 - PROMMO Trial: Oral Misoprostol vs IV Oxytocin Early Phase 1
Completed NCT04597333 - Labor Induction After Failed Induction With Dinoprostone. N/A
Completed NCT03682718 - Vaginal Misoprostol With Intracervical Foley Catheter in Induction of Labor Phase 4
Recruiting NCT03533699 - A Comparison Between the Effect of Oxytocin Only and Oxytocin Plus Propranolol on Induction of Labor in Term Pregnancy N/A
Recruiting NCT05187247 - VR Glasses During Induction of Labour for Pain and Anxiety Relieve N/A
Active, not recruiting NCT02975167 - Patient Satisfaction During Outpatient Versus Inpatient Foley Catheter Induction of Labor N/A
Recruiting NCT05079841 - The Stimulation To Induce Mothers Study Phase 4
Not yet recruiting NCT06375746 - The Impact of a Customized Informative Video Prior to Induction of Labor on Anxiety Relieve - a Randomized Controlled Trial Phase 3
Completed NCT03822052 - The Use of D5LR Versus LR for Induction of Labor and Time to Delivery in Multiparous and Primiparous Patient's With Favorable and Unfavorable Bishop's Scores N/A
Completed NCT04220320 - The Success of Labor Induction Based on a Modified BISHOP Score.
Withdrawn NCT04739683 - Cervical Ripening With Foley Bulb Versus Dilapan-S at Home N/A
Completed NCT03086967 - Cervical Ripening With a Double-lumen Balloon Catheter for Six Versus Twelve Hours N/A
Completed NCT04299854 - Modality of Induction of Labor in Obese Women at Term (MODOBAT)
Completed NCT03944187 - Sonographic Assessment for Prediction of Labor Induction Success
Recruiting NCT03928899 - The Best Timing of Delivery in Women With GDM Study N/A
Terminated NCT04011098 - Improving Labour Induction Analgesia: Epidural Fentanyl Bolus at Epidural Initiation for Induction of Labour Phase 1
Completed NCT02952807 - Vaginal Misoprostol and Foley Catheter for Induction of Labor Phase 2