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Clinical Trials/NCT05823610
NCT05823610
Not yet recruiting
Not Applicable

Intrapartum Ultrasonography in Evaluation of the Progress of Labor

Assiut University0 sites300 target enrollmentJune 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Progress pf Labor
Sponsor
Assiut University
Enrollment
300
Primary Endpoint
compare the intrapartum sonographic parameters between women who had spontaneous vaginal delivery (SVD) vs those who required CS
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

The optimal management of the second stage of labor is a subject of an ongoing debate. It is well established that prolonged second stage of labor is associated with increased maternal and neonatal morbidity.

Diagnosing the onset of labour is one of the most critical and complex judgments made by care providers in the delivery room. Measurement of cervical dilatation is considered the most crucial parameter for labour progress during childbirth and the main reason for doing digital vaginal examination (DVE) in women with signs of labour onset.

DVE was the most common method for measuring cervical dilatation in the past and has been the gold standard for assessing labour progress. However, it can be subjective, inaccurate, and uncomfortable for women. Also, only 50% of assessments are accurate, and there is an increased risk of infection with frequent DVE. Therefore, vaginal examination cannot be a correct scale for measuring cervical dilatation, mainly when done by different examiners. Because of the poor reliability and pain associated with DVE, the use of intrapartum ultrasound to measure cervical dilation has been suggested as an alternative method. Abdominal, vaginal, trans-labial, and trans-perineal 2D and 3D ultrasounds have been used to measure cervical dilatation during labour.

Registry
clinicaltrials.gov
Start Date
June 2023
End Date
September 2025
Last Updated
3 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ahmed Mohamed Abbas

principal investigator

Assiut University

Eligibility Criteria

Inclusion Criteria

  • Primigravida patients
  • At the onset of active phase
  • Cephalic vertex presentation
  • Estimated Fetal Weight 3Kg - 4Kg
  • Gestational Age ≥37 weeks

Exclusion Criteria

  • Multiple Pregnancy
  • Patients refused to participate in our study
  • Induced labor
  • Any Obstetrical Complication or Disease
  • Malpresentation

Outcomes

Primary Outcomes

compare the intrapartum sonographic parameters between women who had spontaneous vaginal delivery (SVD) vs those who required CS

Time Frame: one hour

Ultrasound evaluation of the parameters of progress of labour

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