- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04130139
Benefits of an Oocyte Pickup Simulation Training Program
October 15, 2019 updated by: University Hospital, Angers
Benefits of an Oocyte Pickup Simulation Training Program Using a High-fidelity Simulator for Obstetrics and Gynecology Residents
The primary objective of this study was to evaluate oocyte pick up simulation training program for teaching residents.
The secondary objectives were to evaluate resident satisfaction and the overall current state of oocyte pick up training in France.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
simulation workshop using PickupSim simulator. inclusion: obstetrics and gynecology residents from France simulator: 7 scenarios available
1 simulation training/resident main outcome: successful completion of the scenario (oocyte retrieval rate >=70%) secondary outcome: time for completion, complications, satisfaction survey
Study Type
Observational
Enrollment (Actual)
46
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Angers, France, 49100
- Centre Hospitalier Universitaire Angers
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
obstetrics and gynecology residents from France participating in a national training conference organized by the national college of french gynecologists and obstetricians.
Description
Inclusion Criteria:
- obstetrics and gynecology residents
- french residents
Exclusion Criteria:
- no
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
residents
obstetrics and gynecology residents from France with or without previous experience in oocyte pick up
|
oocyte pick up simulation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
successful scenario
Time Frame: 1 day
|
oocyte retrieval rate >=70%
|
1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
completion time
Time Frame: 1 day
|
time to successfully complete the scenario
|
1 day
|
|
complications
Time Frame: 1 day
|
complications that may occurs during the simulation training (lesions of vitals organs, forget to change collection tubes)
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Pierre Emmanuel Bouet, MD, Centre Hospitalier D'Angers
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 1, 2017
Primary Completion (Actual)
September 1, 2017
Study Completion (Anticipated)
November 1, 2019
Study Registration Dates
First Submitted
October 10, 2019
First Submitted That Met QC Criteria
October 15, 2019
First Posted (Actual)
October 17, 2019
Study Record Updates
Last Update Posted (Actual)
October 17, 2019
Last Update Submitted That Met QC Criteria
October 15, 2019
Last Verified
October 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- Pickupsim
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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