UnknownNot Applicable

Impact of Simulation Training for Obstetrics-gynecology Residents.

Switzerland68 participantsStarted 2018-08-28

Plain-language summary

The main objective of the study is to evaluate the benefit of simulator training for learning external cephalic version (ECV) or vacuum assisted vaginal delivery (hereafter vacuum extraction \[VE\]) for obstetrics-gynecology residents. The primary outcome of this randomized control trial is to evaluate the impact of simulation training on the success of ECV and VE.

Who can participate

Age range18 Years

SexALL

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Inclusion Criteria: * Being a resident or consultant working in the gynecology and obstetrics department of the hospital * Agreeing to participate in the study by signing an informed consent form Exclusion Criteria: * Having performed several ECV or VE simulation training (more than 1 session each) before the recruitment * Having already performed more than 20 ECV and more than 20 VE during clinical practice before recruitment. * Having a planned clinical activity in the delivery room which does not allow to perform at least 1 ECV or 1 VE during the study period.

What they're measuring

Success rate of the ECV in the participant clinical practice

Timeframe: 6 months

Success rate of the VE in the participant clinical practice

Timeframe: 6 months

Trial details

NCT IDNCT03848975

SponsorUniversity Hospital, Geneva

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-11-01

Contact for this trial

Lorraine Grangier, MD

+41795535019 lorraine.grangier@hcuge.ch

View on ClinicalTrials.gov More Simulation Training trials