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Active, not recruiting Observational

Robson Classification System Monitoring and Auditing Caesrean Section Rates

NCT07504328 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2026-02-01
Last updated
2026-03-31

Condition(s) studied

Caesrean Section RatesRobson Classification

Investigational drug(s) / intervention(s)

just monitoring and auditing ,so there is no intevention

just monitoring and auditing ,so there is no intevention: just monitoring and auditing ,so there is no intevention

Study summary

Robson Classification System Monitoring and Auditing Caesrean Section Rates

Eligibility

Sex
FEMALE
Min age
—
Max age
—
Healthy volunteers
No
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

Primary outcome measure(s)

  • Change in overall Caesarean section rate — 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

Trial sites (1)

FacilityCityRegionStatus
Sohag University Sohag Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07504328 on ClinicalTrials.gov ↗ ← All trials in Egypt