Robson Ten-Group Classification Study of Cesarean Section Rates in Assiut Hospitals

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-45
SponsorAssiut University

About this trial

Cesarean section (C-section) rates have increased worldwide, and Egypt is among the countries with the highest rates. In some hospitals, more than half of all births are done by cesarean delivery. The World Health Organization (WHO) recommends using the "Robson Ten Group Classification System" to better understand and compare C-section rates.

This study will use the Robson classification system to evaluate the rate of cesarean deliveries in two hospitals in Assiut, Egypt: Assiut University Hospital and Assiut General Hospital. The study will collect information from medical records of women who delivered by cesarean section between January and December 2026.

The main goal is to identify which groups of women contribute most to the high C-section rate and to compare practices between the two hospitals. The study will also look at outcomes for both mothers and newborns. By doing this, we hope to provide useful information that can help improve obstetric care, reduce unnecessary cesarean deliveries, and improve health outcomes for mothers and babies in Egypt.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Women who delivered by cesarean section at Assiut University Hospital or Assiut General Hospital during the study period (January-December 2026).

Disqualifiers

Vaginal deliveries.

Trial population

Women delivering by cesarean section at Assiut University Hospital and Assiut General Hospital in Assiut, Egypt, between January and December 2026. Data will be collected from medical records and classified using the Robson Ten Group Classification System.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • No Intervention (subjects were previously treated with Onglyza®)

    Other intervention

    no intervention

Treatment groups

770 Participants
are divided into 1 treatment group
Group A: Cesarean Deliveries in Assiut Hospitals1 intervention

Trial outcomes

Primary outcomes

1

Distribution of cesarean deliveries by Robson Ten Group Classification

Proportion of cesarean section deliveries categorized into the ten Robson groups, calculated as a percentage of total cesarean deliveries. The main objective is to identify the groups contributing most to the overall cesarean section rate.

Time frame
January 2026 - December 2026

Secondary outcomes

1

Comparison of cesarean section rates within Robson groups between hospitals

Rate and relative contribution of each Robson group will be compared between Assiut University Hospital and Assiut General Hospital.

Time frame
January 2026 - December 2026

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: