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Not yet recruiting NCT06680804

Factors Affecting Success of Vaginal Birth After Cesarean Section

Observational Vaginal Delivery

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: chance for vaginal delivery..
Who it may be relevant to
Registry conditions: Vaginal Delivery. Basic parameters: 20 years — 40 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Factors Affecting Success of Vaginal Birth After Cesarean Section in Sohag University Hospitals

Overview

Factors affecting Success of Vaginal Birth After Cesarean Section in Sohag University Hospitals

Detailed description

* Clinical data will be collected from the participants including demographic details such as age, maternal age, parity, BMI, gestational age based on last menstrual period or early ultrasound scans available. * Full medical and surgical history, previous CS details as an indication, and previous complications. * Patients' clinical abdominal and per vaginal examination on admission (cervical dilatation, effacement head station, and position). * CTG attached on admission (to exclude fetal distress). * Laboratory investigations that will be done before delivery and postpartum, Labor progress on the partogram will be assessed as regard duration of both first and second stages of labor if any instrumental delivery will be done. * Radiology investigations such as US. * Records for patients' vital signs, fetal cardiac activity during labor, vaginal bleeding, delivery notes, fetal weight, and 5 minutes APGAR score, and any recorded maternal or fetal complications. * If failed VBAC: Causes of failure maternal and fetal outcomes will be recorded and immediate CS to be done

Interventions

  • Other chance for vaginal delivery.
    chance for vaginal delivery in patients who had delivered by Caesarean section in first pregnancy

Primary outcome measures

  • successful vaginal delivery [Time frame: From November 2024 to April 2025]

Eligibility criteria

Inclusion criteria

  • • Age from 20 to 40 years.
  • Time interval more than 1.5 years from previous caesarean section.
  • Single viable full-term pregnancy in vertex presentation.
  • Reactive cardiotocography (CTG) on admission.
  • Spontaneous labor onset.
  • Clinically adequate pelvis.
  • Single fetus
  • Average AFI fetus

Exclusion criteria

  • • Women with previous upper segment cesarean section or hysterotomy scar.
  • Any obstetric complications such as fetal malpresentation, placenta previa, or medical disorders like diabetes mellitus or preeclampsia.
  • Presence of any signs and symptoms of scar dehiscence or ruptured uterus, known uterine fibroid or anomaly.
  • Suspected fetal macrosomia (weight more than 4 kg).
  • Multifetal pregnancy.
  • Parturient women who refused the trial of vaginal birth after caesarean section.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06680804 · soh-Ned-15-10_9MS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗