Robson Classification System Monitoring and Auditing Caesrean Section Rates

March 25, 2026 updated by: Mohamed Tarek Ahmed Zaghlol, Sohag University

Robson Classification System Monitoring and Auditing Caesrean Section Rates in Sohag Governate Hospitals

Robson Classification System Monitoring and Auditing Caesrean Section Rates

Study Overview

Study Type

Observational

Enrollment (Estimated)

300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Sohag, Egypt, 82524
        • Sohag University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

pregnant women at >=28 weeks gestaion age.

Description

Inclusion Criteria:

  • All pregnant women delivering at ≥ 28 weeks gestation.
  • Singleton or multiple pregnancy.
  • Cephalic, Breech, or transverse lie.

Exclusion Criteria:

  • Gestational age < 28 weeks.
  • Intrauterine fetal demises before admission

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Pregnant Women delivering at>28weeks gestaion
Pregnant Women delivering at>28weeks gestaion (interuterine fetal demises before admission are excluded)
just monitoring and auditing ,so there is no intevention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in overall Caesarean section rate
Time Frame: until 1/february/2027

All eligible deliveries during the study period will be included (total coverage sampling).

Collection of baseline data on mode of delivery. Calculation of CS rate and indications. Classification of women retrospectively into Robson groups. Monthly audit meetings to discuss CS indications per Robson group. Data Collection

Data will be collected using a structured sheet including:

Maternal age Parity Gestational age Onset of labor Fetal presentation Number of fetuses Mode of delivery Indication of CS Robson group Maternal outcome Neonatal outcome

until 1/february/2027

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cs rate in each Robson group. Change in primary Cs rate. Change in repeat Cs rate. Matenal morbidity. Neonatal outcomes(Apgar,NICU admission)
Time Frame: until 1/february/2027
Cs rate in each Robson group Change in primary Cs rate. Change in repeat Cs rate. Matenal morbidity. Neonatal outcomes(Apgar,NICU admission)
until 1/february/2027

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Ahmed Abd El Raheem Ahmed, Sohag University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 1, 2026

Primary Completion (Estimated)

January 1, 2027

Study Completion (Estimated)

February 1, 2027

Study Registration Dates

First Submitted

March 18, 2026

First Submitted That Met QC Criteria

March 25, 2026

First Posted (Actual)

March 31, 2026

Study Record Updates

Last Update Posted (Actual)

March 31, 2026

Last Update Submitted That Met QC Criteria

March 25, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • Soh-Med-26-3-11MS

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Caesrean Section Rates

Clinical Trials on just monitoring and auditing ,so there is no intevention

Subscribe