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Safety and Efficacy of the Knee-T-nol Anterior Cruciate Ligament (ACL) Prosthesis

Anterior Cruciate Ligament Rupture Clinical Trial

Official title:
A Single Arm, Prospective, Single Center, Study To Evaluate The Safety And Efficacy Of Tavor ACL Prosthesis In Patient With ACL Rupture

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

  • Anterior Cruciate Ligament Rupture
  • Rupture
Clinical Trial Details
NCT number NCT01450332
Study type Interventional
Source Tavor Ltd.
Contact Jonathan S Yalom, B.Sc.
Phone +972-9-7733910
Email jonathan@tavormed.com
Status Recruiting
Phase N/A
Start date March 2011
Completion date January 2013
View Details
See also
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Completed NCT01267435 - Evaluation of Tibial and Femoral Tunnel Position After Arthroscopic Reconstruction of the Anterior Cruciate Ligament Phase 2
Recruiting NCT06430775 - Exploring Prolonged AMR in ACL Reconstructed Patients