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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