CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 409 enrolled
Drug / intervention
Quality Improvement Projectother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03387189
NCT03387189N/ACompleted
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Morbidity of Second Stage Cesarean Sections Before and After Provider Completion of Simulation Education at Regions Hospital

HealthPartners Institute·observational·Posted Jan 2, 2018·Updated Nov 21, 2024

In Brief

An observational study evaluating Quality Improvement Project for Obstetric Labor Complications and Cesarean Section. Completed, enrolled 409 participants across 1 site.

Detailed Summary

This study is an evaluation of a Quality Improvement (QI) project addressing delivery of the impacted fetal head being conducted at Regions Hospital. This study aims to determine the morbidity of second stage cesarean deliveries before and after implementation of simulation protocols that address delivery of the impacted fetal head for Ob/gyn surgeons, nursing staff, and surgical technicians at Regions Hospital.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsObstetric Labor Complications, Cesarean Section
CountriesUnited States
CollaboratorsRegions Hospital

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedJan 2, 2018
Enrollment StartJan 1, 2018
Primary CompletionJun 30, 2019
TodayJul 2, 2026
Enrollment to primary: 1.5 yearsPosted 8.5 years ago

Interventions

Quality Improvement Projectother

Simulation education conducted at Regions Hospital for a Quality Improvement project on delivery of impacted fetal head at cesarean section. This is a department-wide, simulation-based educational training required for all Regions Hospital Birth Center staff physicians, residents, nursing staff, and surgical techs.