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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01808807
Other study ID # 101110-F
Secondary ID
Status Completed
Phase N/A
First received December 11, 2012
Last updated August 16, 2013
Start date December 2012

Study information

Verified date March 2013
Source Far Eastern Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Institutional Review Board
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 4000
Est. completion date
Est. primary completion date April 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 15 Years to 47 Years
Eligibility 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 Design

Observational Model: Case Control, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan Far Eastern Memorial Hospital Pan-Chiao,

Sponsors (1)

Lead Sponsor Collaborator
Far Eastern Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary the impact of the cesarean section rate audit 1 month No
See also
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