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Comparison of da Vinci Simulator vs LapSim Simulator

Not Applicable
Withdrawn
Conditions
Robotic Surgery Training
Laparoscopy Training
Interventions
Other: da Vinci Skills Simulator®
Other: LapSim®
Other: Dry lab box laparoscopic training
Registration Number
NCT03079908
Lead Sponsor
Klinik für Allgemein- und Viszeralchirurgie, Department Chirurgie, Luzerner Kantonsspital
Brief Summary

Virtual reality surgical simulators (VRSS) are gaining popularity for general surgery training, both for conventional laparoscopic and robotically-assisted surgery. Although numerous studies have analysed the impact of VRSS training on surgical skills, there is a lack of data regarding the comparison of robotic VRSS (RVRSS) and laparoscopic VRSS (LVRSS) training on conventional laparoscopic skills among subjects with no prior surgical experience. The hypothesis of the present study is that RVRSS could improve conventional laparoscopic skills as much as laparoscopic LVRSS among naïve subjects

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Healthy medical students aged 20 to 30 years old
Exclusion Criteria
  • No prior surgical, laparoscopic or robotic experience
  • No previously known severe learning disability or mental deficiency
  • No handicap limiting the usage of one or both upper limb(s)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Da Vinci Skills Simulator®da Vinci Skills Simulator®Participants in this group will undergo robotic virtual reality surgical simulator training (Da Vinci Mimics) and will subsequently be evaluated on a dry lab laparoscopic box
LapSim®LapSim®Participants in this group will undergo laparoscopic virtual reality surgical simulator Training (LapSim) and will subsequently be evaluated on a dry lab laparoscopic box
Dry lab box laparoscopic trainingDry lab box laparoscopic trainingParticipants in this group will undergo dry lab box laparoscopic training only
Primary Outcome Measures
NameTimeMethod
Exercises timesWithin 1 day after randomization / data will be presented after completion of the study (an average of 9 months)

Time to realize each training exercise as well as the final evaluation exercise

Secondary Outcome Measures
NameTimeMethod
Instruments collisionsWithin 1 day after randomization / data will be presented after completion of the study (an average of 9 months)

Number of collisions between the different instruments used to perform each training exercise as well as the final evaluation exercise

Objects dropsWithin 1 day after randomization / data will be presented after completion of the study (an average of 9 months)

Number of time objects were unwillingly dropped during each training exercise as well as the final evaluation exercise

Objects out of viewWithin 1 day after randomization / data will be presented after completion of the study (an average of 9 months)

Number of times one or both instruments or objects used for the exercises were out of the viewing field during each training exercise as well as the final evaluation exercise

Trial Locations

Locations (1)

Luzern Kantonsspital Luzern

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Luzern, Switzerland

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