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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02216448
Other study ID # SHEBA-14-1236-DP-CTIL
Secondary ID
Status Withdrawn
Phase N/A
First received July 9, 2014
Last updated April 19, 2018
Start date September 2014
Est. completion date December 2017

Study information

Verified date April 2018
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare between two groups of residents with basic arthroscopic skills in diagnostic knee arthroscopy. The first group will train on a knee arthroscopic simulator in a lab, and the second group will perform diagnostic knee arthroscopy in the operating room. Both groups will be assessed by senior arthroscopy surgeon in the operating room based on selected competencies following the Global Rating System.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2017
Est. primary completion date December 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Orthopedic residents

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Training knee simulator
Training in a lab on a virtual reality knee arthroscopy simulator
OR Training
Training on diagnostic knee arthroscopy in the OR

Locations

Country Name City State
Israel Sheba Tel Hashomer Ramat Gan

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Global rating scale About 3 months will be needed for both study arms to complete the training in the arthroscopy lab and in the OR. Then, both will be assessed by the global rating scale for arthroscopy. completion of training
Secondary simulator parameters Secondary outcome measures are technical parameters provided by the simulator for each trainee. At the end of the training sessions, about 3 months from the beginning of the study, this parameters can be collected. Completion of training