Benefits of an Oocyte Pickup Simulation Training Program

• Sponsor: University Hospital, Angers (Other)
• Overall Status: Unknown status
• CT.gov ID: NCT04130139
• Collaborator: (none)
• Enrollment: 46
• Location: 1
• Anticipated Duration (Months): 27
• Patients Per Site Per Month: 1.7

Study Details

Study Description

Brief Summary

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.

Condition or Disease	Intervention/Treatment	Phase
Simulation Training; IVf; Education	Other: oocyte pick up simulator

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 Design

• Study Type: Observational
• Actual Enrollment: 46 participants
• Observational Model: Cohort
• Time Perspective: Prospective
• Official Title: Benefits of an Oocyte Pickup Simulation Training Program Using a High-fidelity Simulator for Obstetrics and Gynecology Residents
• Actual Study Start Date: Aug 1, 2017
• Actual Primary Completion Date: Sep 1, 2017
• Anticipated Study Completion Date: Nov 1, 2019

Arms and Interventions

Arm	Intervention/Treatment
residents obstetrics and gynecology residents from France with or without previous experience in oocyte pick up	Other: oocyte pick up simulator; oocyte pick up simulation

Outcome Measures

Primary Outcome Measures

1. successful scenario [1 day]

   oocyte retrieval rate >=70%

Secondary Outcome Measures

1. completion time [1 day]

   time to successfully complete the scenario

2. complications [1 day]

   complications that may occurs during the simulation training (lesions of vitals organs, forget to change collection tubes)

Eligibility Criteria

Criteria

• Ages Eligible for Study: N/A and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

• obstetrics and gynecology residents

• french residents

Exclusion Criteria:

• no

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Centre Hospitalier Universitaire Angers	Angers		France	49100

Sponsors and Collaborators

• University Hospital, Angers

Investigators

• Principal Investigator: Pierre Emmanuel Bouet, MD, Centre hospitalier d'Angers

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: University Hospital, Angers
• ClinicalTrials.gov Identifier: NCT04130139
• Other Study ID Numbers: Pickupsim
• First Posted: Oct 17, 2019
• Last Update Posted: Oct 17, 2019
• Last Verified: Oct 1, 2019

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

Study Results

No Results Posted as of Oct 17, 2019