NCT01808807

Brief 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.

Trial Health

80
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
4,000

participants targeted

Target at P75+ for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2012

Completed
10 days until next milestone

First Submitted

Initial submission to the registry

December 11, 2012

Completed
3 months until next milestone

First Posted

Study publicly available on registry

March 11, 2013

Completed
21 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2013

Completed
Last Updated

August 19, 2013

Status Verified

March 1, 2013

Enrollment Period

4 months

First QC Date

December 11, 2012

Last Update Submit

August 16, 2013

Conditions

Cesarean Section

Keywords

cesarean section ratethe cesarean section rate audit

Outcome Measures

Primary Outcomes (1)

  • the impact of the cesarean section rate audit

    1 month

Study Arms (1)

cesarean section rate after audit

cesarean section rate after audit

Eligibility Criteria

Age15 Years - 47 Years
Sexfemale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodProbability Sample
Study Population

pregnant women who delivered in a medical center will be included retrospectively in this study

You may qualify if:

  • All pregnant women who delivered in a medical center will be included retrospectively in this study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Far Eastern Memorial Hospital

Banqiao District, Taiwan

Location

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Chief, Department of Obstetrics & Gynecology

Study Record Dates

First Submitted

December 11, 2012

First Posted

March 11, 2013

Study Start

December 1, 2012

Primary Completion

April 1, 2013

Last Updated

August 19, 2013

Record last verified: 2013-03

Locations

TW(1)