Detecting the Most Efficient Residency Time for Laparoscopic Simulators
NCT ID: NCT05302622
Last Updated: 2022-03-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
27 participants
INTERVENTIONAL
2021-10-01
2022-06-15
Brief Summary
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This study planned as a prospective study. There will be three group which include ob/gyn residents. The residents will choose based on their residency year and surgery skills. 1. The residents who makes surgeries both laparoscopic and laparotomic, 2. The residents who makes surgeries only laparotomic, 3. The residents who won't any gynecologic surgery The data of surgery time, complications and movement numbers will take from the simulator. Tubal ligation and salpingooferectomy choose for the surgery examples. The simulation results of participants will compare and try to find the best improvement term for residency.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Group 1
Have surgical experience both laparoscopy and laparotomy and senior resident
There is no intervention planning
There is no intervention planning
Group 2
Have surgical skills only laparotomic gynecologic procedures and in the middle of his/her residency
There is no intervention planning
There is no intervention planning
Group 3
Have no surgical experience on gynecologic procedures and newbie residents
There is no intervention planning
There is no intervention planning
Interventions
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There is no intervention planning
There is no intervention planning
Eligibility Criteria
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Inclusion Criteria
* Should except to participate study
Exclusion Criteria
24 Years
30 Years
ALL
No
Sponsors
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Tepecik Training and Research Hospital
OTHER
Responsible Party
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Ahkam Göksel Kanmaz
Associated Professor
Locations
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Tepecik Education and Research Hospital
Izmir, , Turkey (Türkiye)
Countries
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Other Identifiers
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2021/10-48
Identifier Type: -
Identifier Source: org_study_id
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