Engagement of Fetal Head as a Predictor of a Successful Vaginal Delivery in Primigravidas Presented in Early Labor.
NCT ID: NCT05084326
Last Updated: 2022-01-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
226 participants
OBSERVATIONAL
2020-11-03
2021-11-20
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Reverse Breech Extraction Versus Push Technique for Fetal Delivery When Fetal Head is Deeply Impacted in the Pelvis During CS on A Fully Dilated Cervix
NCT05707650
Cephalic Version by Acupuncture for Breech Presentation
NCT00813683
Prediction of Delivery Mode by Ultrasound-assessed Fetal Position in Nulliparous Women With Prolonged First Stage of Labor.
NCT05206409
Sonographic Parameters and Risk of Antepartum Hemorrhage in Asymptomatic Women With Placenta Previa: A Cohort Study
NCT05802251
Ultrasound Parameters for the Outcome Prediction of External Cephalic Version for Fetuses with Breech Presentation
NCT06593795
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
while assessment of fetal head station, status of membrane should be evaluated and noted.
Engagement will be assessed by vaginal examination as described by Müller in 1868 , assumes that when the leading edge of the vertex is felt at the level of the ischial spines, the biparietal diameter will have just passed through the pelvic brim. The leading edge of the vertex at the level of the ischial spines is designated as being at station 0. If the leading edge is 1 cm below the level of the spines, this is referred to as station +1. Usually, a head on the pelvic floor is at station +4 or +5.
Uengaged head is still 2 cm above the level of the spines is at station -2, and so on.
The aim of this study will be to determine if primigravida patients with unengaged head after spontaneous onset of labor are at increased risk of cesarean section.
The patients will be admitted in the labour room. Name, age and detailed history will be noted A thorough general examination and systemic examination will be done to determine the fundal height, the baby's lie, presentation, position, engagement of the presenting part, and frequency and duration of contractions, auscultation of the fetal heart rate for a minimum of 1 minute immediately after a contraction.
A vaginal examination will be offered for more assessment of pelvic status, cervical dilation (in cm) and effacement, position of fetal head and status of membrane will be evaluated and noted.
Assessment of labor progress will be done by digital examination : to document cervical dilation, effacement, and fetal station are usually routinely performed:
* At four hour intervals in the first stage
* Prior to administering analgesia/anesthesia\*
* When the parturient feels the urge to push (to determine whether the cervix is fully dilated)
* At one hour intervals in the second stage
* If fetal heart rate abnormalities occur " to evaluate for complications such as cord prolapse "
* All patients should be counselled and offered Epidural anesthesia during first and second stage of labor.
Observations during the established frst stage:
1. Half-hourly documentation of frequency of contractions
2. Hourly pulse
3. 4-hourly temperature and blood pressure
4. A vaginal examination 4-hourly or if there is concern about progress
If delay is established in first stage of labour of cervical dilatation of less than 2 cm in 4 hours for frst labour , amniotomy should be considered for all women with intact membranes increase the strength and pain of contractions, in normally progressing labour, do not perform amniotomy routinely.
vaginal examination 2 hours later, and diagnose delay if progress is less than 1 cm.
increase the strength and pain of contractions, vaginal examination 2 hours later, and diagnose delay if progress is less than 1 cm.
Decision about management options of oxytocin augmentation according NICE guidelines should considered.
According to RCOG guidelines, we will use a low-dose protocol for all patients, by adding 10 IU oxytocin to 1 litre of 0.9% normal saline.
Electronic fetal monitoring will be performed for a minimum of 20 minutes before starting oxytocin, and will be continued until the baby is delivered, intervention will be according to interpretation of CTG.
According to NICE guidelines, vaginal examination 4 hours after starting oxytocin in established labour:
* If cervical dilatation has increased by less than 2 cm after 4 hours of oxytocin, further obstetric review is required to assess the need for caesarean section.
* If cervical dilatation has increased by 2 cm or more, advise 4-hourly vaginal examinations.
Observations during the second stage:
1. Half-hourly documentation of the frequency of contractions.
2. Hourly blood pressure.
3. Continued 4-hourly temperature.
4. Frequency of passing urine .
5. A vaginal examination hourly in the active second stage.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Mohamedabosena
Engagement of fetal head as a predictor of a successful vaginal delivery
In addition to the fetal lie, presentation, and position, the level or station of the presenting part in the maternal pelvis is an important factors in the labor process.
In primigravida, Delayed engagement of fetal head has been theorized that it is more likely in women with a possible cephalo-pelvic disproportion, so far they are associated with higher risk of cervical dystocia, which led to increased rate of caesarean section.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Engagement of fetal head as a predictor of a successful vaginal delivery
In addition to the fetal lie, presentation, and position, the level or station of the presenting part in the maternal pelvis is an important factors in the labor process.
In primigravida, Delayed engagement of fetal head has been theorized that it is more likely in women with a possible cephalo-pelvic disproportion, so far they are associated with higher risk of cervical dystocia, which led to increased rate of caesarean section.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Expected foetal birth weight of 2.5-4.0 kg on USG at term.
* Singleton live pregnancy.
* Cephalic presentation.
* Cervical dilatation of =/\< 4cms.
* Reactive CTG at onset of labour.
* Confirmation of ROM by Direct visualization or Fern test.
Exclusion Criteria
* Previous uterine surgery " upper segment ".
* Pregnancy complications like antepartum haemorrhage, pregnancy induced hypertension, gestational diabetes mellitus, IUGR.
* Fetal congenital anomalies.
* Abnormal or non reassuring fetal CTG at term or at onset of labour.
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ain Shams University
OTHER
mohamed abosena
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
mohamed abosena
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Mohamed M sami, Consultant
Role: STUDY_DIRECTOR
As.Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ain Shams university
Cairo, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
AinShamsU Hos
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.