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More info
You can access this
clinical trial
if you have
Anterior Cruciate Ligament Rupture
and you are
between 18 and 65
years old
The phase for this study is not defined.
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The purpose

The study is designed to evaluate the safety and efficacy of implanting the Tavor ACL prosthesis in patients with a ruptured ACL by improvement of healing kinetics as well as major adverse treatment events (AEs). it is designed to test the hypothesis that there is a difference in healing kinetics of ACL deficient knees treated by ACL reconstruction using autografts and those in which such procedure was performed with the Tavor prosthesis.

Provided treatments

  • Device: Knee-T-Nol

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT01450332. The sponsor of the trial is Tavor Ltd. and it is looking for 20 volunteers for the current phase.
Official trial title:
A Single Arm, Prospective, Single Center, Study To Evaluate The Safety And Efficacy Of Tavor ACL Prosthesis In Patient With ACL Rupture