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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
WITHDRAWN
NA
INTERVENTIONAL
2014-09-30
2017-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Single Cutting Guides System for the Installation of a Total Knee Replacement
NCT02429245
Autologous Cartilage Implantation vs Arthroscopic Debridement
NCT02636881
Non-Invasive Distractor During Knee Arthroscopy
NCT06458816
Kinematic Comparison of Vanguard XP and Vanguard CR Total Knee Arthroplasties
NCT02921594
Use of the LRU Pillow in the Acute Setting Following Total Knee Arthroplasty
NCT01814033
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
OTHER
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
simulator training
Training knee simulator in Lab
Training knee simulator
Training in a lab on a virtual reality knee arthroscopy simulator
OR training
Training in the OR - 2 knee arthroscopies.
OR Training
Training on diagnostic knee arthroscopy in the OR
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Training knee simulator
Training in a lab on a virtual reality knee arthroscopy simulator
OR Training
Training on diagnostic knee arthroscopy in the OR
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
80 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Sheba Medical Center
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Dr. Dan Prat MD
MD
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Sheba Tel Hashomer
Ramat Gan, , Israel
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
SHEBA-14-1236-DP-CTIL
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.