Restor3D: Osteoarthritis trials

The registry lists 16 Osteoarthritis studies with Restor3D as lead sponsor. 0 are open to participants now and 5 have results posted.

No phase 16(a study in two phases counts in both)

Studies

Open to participants first, then studies with results posted, then the rest; newest registration first within each.

• A Prospective Study to Evaluate the iTotal Knee and iPoly XE Tibial InsertsTerminatedNCT03289754Not applicableResults posted
• A Multicenter Study to Evaluate Functional Outcome After Knee ReplacementTerminatedNCT02494544Not applicableResults posted
• Study Comparing Fit of the iTotal Versus Standard Total Knee ImplantsTerminatedNCT01861028Results posted
• Comparison of Knee Kinematics for Subjects Implanted With Either a ConforMIS or Traditional Knee ImplantCompletedNCT01717001Results posted
• A Retrospective Study of the iTotal CR Knee Replacement SystemCompletedNCT01564654Results posted
• A Retrospective Study to Evaluate the ConforMIS iTotal® Posterior Stabilized (PS) Knee Replacement SystemCompletedNCT03289000
• A Retrospective Study to Evaluate the ConforMIS iUni, iDuo & iTotal® KRSCompletedNCT03152357
• A Prospective Study to Evaluate the ConforMIS iTotal® (PS) Knee Replacement SystemTerminatedNCT03152162
• A Single Time-Point Study to Evaluate the ConforMIS iTotal (PS) Knee Replacement System Versus Off-the-ShelfTerminatedNCT03146819
• A Single Time-Point Study to Evaluate the ConforMIS iTotal® (CR) Knee Versus Off-the-ShelfCompletedNCT02251522
• Total Knee Arthroplasty Functional Outcomes Study Research DesignTerminatedNCT02228538
• Costs and Benefits of ConforMIS iTotal® Knee Replacement System Versus Standard Total KneeCompletedNCT01899417
• iUni G2+ Prospective StudyTerminatedNCT01820676
• A Prospective, Multicenter Study to Evaluate the ConforMIS iTotal® (CR) Knee Replacement SystemTerminatedNCT01820650
• Study of the ConforMIS iDuo(R) G2TerminatedNCT01564641
• Multi-Center Study to Evaluate the ConforMIS iUni Knee ImplantTerminatedNCT01117571