NCT06680804

Brief Summary

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

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Dec 2024

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 7, 2024

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 8, 2024

Completed
23 days until next milestone

Study Start

First participant enrolled

December 1, 2024

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2025

Completed
Last Updated

November 8, 2024

Status Verified

November 1, 2024

Enrollment Period

5 months

First QC Date

November 7, 2024

Last Update Submit

November 7, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • successful vaginal delivery

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

    From November 2024 to April 2025

Study Arms (2)

Group I: Successful VBAC group

Successful VBAC group whose take chance for vaginal delivery.

Other: chance for vaginal delivery.

Group II: Failed VBAC group

Failed VBAC group whose take chance for vaginal delivery.

Other: chance for vaginal delivery.

Interventions

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

Group I: Successful VBAC groupGroup II: Failed VBAC group

Eligibility Criteria

Age20 Years - 40 Years
Sexfemale
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

All patients admitted for vaginal delivery with previous lower segment cesarean section . Age from 20 to 40 years.Time interval more than 1.5 years from previous caesarean section.

You may qualify if:

  • 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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Nahla Rashwan ezzeldine, master

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Resident at obstetrics and gynecology , sohag university

Study Record Dates

First Submitted

November 7, 2024

First Posted

November 8, 2024

Study Start

December 1, 2024

Primary Completion

May 1, 2025

Study Completion

May 1, 2025

Last Updated

November 8, 2024

Record last verified: 2024-11

Data Sharing

IPD Sharing
Will not share