Induction of Labor Affected Fetus / Newborn Clinical Trial
Official title:
Outcomes of Induction of Labor: a Prospective Multi-center Study
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.
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.
;
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 |