- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07504328
Robson Classification System Monitoring and Auditing Caesrean Section Rates
Robson Classification System Monitoring and Auditing Caesrean Section Rates in Sohag Governate Hospitals
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
-
Sohag, Egypt, 82524
- Sohag University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
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
Sponsor
Investigators
- Study Director: Ahmed Abd El Raheem Ahmed, Sohag University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
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