NCT04130139

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.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
46

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Aug 2017

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
unknown

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2017

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2017

Completed
2.1 years until next milestone

First Submitted

Initial submission to the registry

October 10, 2019

Completed
7 days until next milestone

First Posted

Study publicly available on registry

October 17, 2019

Completed
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2019

Completed
Last Updated

October 17, 2019

Status Verified

October 1, 2019

Enrollment Period

1 month

First QC Date

October 10, 2019

Last Update Submit

October 15, 2019

Conditions

Simulation TrainingIVfEducation

Outcome Measures

Primary Outcomes (1)

  • successful scenario

    oocyte retrieval rate \>=70%

    1 day

Secondary Outcomes (2)

  • completion time

    1 day

  • complications

    1 day

Study Arms (1)

residents

obstetrics and gynecology residents from France with or without previous experience in oocyte pick up

Other: oocyte pick up simulator

Interventions

oocyte pick up simulatorOTHER

oocyte pick up simulation

residents

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-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.

You may qualify if:

  • obstetrics and gynecology residents
  • french residents

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre Hospitalier Universitaire Angers

Angers, 49100, France

Location

Study Officials

  • Pierre Emmanuel Bouet, MD

    Centre hospitalier d'Angers

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 10, 2019

First Posted

October 17, 2019

Study Start

August 1, 2017

Primary Completion

September 1, 2017

Study Completion

November 1, 2019

Last Updated

October 17, 2019

Record last verified: 2019-10

Locations

FR(1)