- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01808807
Factors Influencing Cesarean Section Rate: Does the Audit Still Work?
To elucidate the audit's effect on caesarean section rate, and also define the factors influencing the caesarean section rate.
From Jan 2007 , pregnant women who delivered in a medical center will be included retrospectively in this study. Our monthly cesarean section audit, focusing on discussing the indications of cesarean section, began from July 2008. Clinical data, indications of cesarean section, and perinatal outcomes were compared between the cases of before and after the audit. Multivariate logistic regression was performed to identify factors affecting cesarean section rate.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Pan-Chiao,, Taiwan
- Far Eastern Memorial Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- All pregnant women who delivered in a medical center will be included retrospectively in this study
Exclusion Criteria:
- All pregnant women who delivered in a medical center will be included retrospectively in this study , no exclusion criteria
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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cesarean section rate after audit
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
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the impact of the cesarean section rate audit
Time Frame: 1 month
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1 month
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 101110-F
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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