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OpenTrials
Completed

NCT Number: 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.

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Key information

Conditions

Cesarean Section

Age range

15 year–47 year

Sex eligibility

Female

Study type

Observational

Primary location

Far Eastern Memorial Hospital

Banqiao District, Taiwan

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. the impact of the cesarean section rate audit

    Time frame: 1 month

Sponsors and collaborators

Lead sponsor

Far Eastern Memorial Hospital

Other

Registry information

Important dates

Study start
2012
Primary completion
2013
First posted
Mar 11, 2013
Registry last updated
Aug 19, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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