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NCT05302622 Clinical Trial

Detecting the Most Efficient Residency Time for Laparoscopic Simulators

Laparoscopy Clinical Trial

Official title:
Determination of the Most Efficacious Period for the Use of Laparoscopic Simulators in Obstetrics and Gynecology Specialty Training

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT05302622
Other study ID # 2021/10-48
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date October 1, 2021
Est. completion date June 15, 2022

Study information
Verified date March 2022
Source Tepecik Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Laparoscopic surgeries is one of the most common surgery in gynecologic procedures. Nowadays there are many laparoscopic simulators for training residents. In this study it is aimed to determine the most efficient residency year for laparoscopic simulators. 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.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 27
Est. completion date June 15, 2022
Est. primary completion date January 1, 2022
Accepts healthy volunteers No
Gender All
Age group 24 Years to 30 Years
Eligibility Inclusion Criteria: - Should be an ob/gyn resident - Should except to participate study Exclusion Criteria: - Not to complete all simulations

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• There is no intervention planning
There is no intervention planning

Locations
Country Name City State
Turkey Tepecik Education and Research Hospital Izmir

Sponsors (1)
Lead Sponsor Collaborator
Tepecik Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Laparoscopic surgical procedures time 6 months
Secondary Movement number for laparoscopic procedures 6 months
Secondary Complication during laparoscopic surgery simulations 6 months
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