Skip to main content
Clinical Trials/NCT06680804
NCT06680804Not yet recruitingNot Applicable

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

Sohag University0 sites1 target enrollmentStarted: December 1, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
1
Primary Endpoint
successful vaginal delivery

Study Overview

Brief Summary

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

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
20 Years to 40 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

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.

Outcomes

Primary Outcomes

successful vaginal delivery

Time Frame: From November 2024 to April 2025

successful vaginal delivery in patients who had delivered by Caesarean section in first pregnancy

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Nahla Rashwan Ezz-eldine

Resident at obstetrics and gynecology , sohag university

Sohag University

Similar Trials