Our grouping. This page groups the registry's lead sponsor names by company — our grouping, not the registry's. It can be wrong or incomplete: an acquired company whose name never mentions its owner may be missing. Use “Something wrong?” under any name below to correct it.
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Restor3D clinical trials
The registry lists 24 studies whose lead sponsor is Restor3D. 2 are recruiting or about to start. Per ClinicalTrials.gov, last updated Sep 21, 2026.
Keep track of what changes. Save the Restor3D studies recruiting or about to start, and get an email each week — studies that open, close, add sites or post results.
Watch these studiesRegistry sponsor names on this page
Each name exactly as ClinicalTrials.gov lists it, and how it relates to Restor3D.
- Restor3D24 studiesSame company
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Focus areas
Conditions Restor3D leads ten or more studies in, by study count. A broader condition is left out when almost all its studies are already in a narrower one listed here.
Studies
Recruiting first, then most recently updated. Showing 24 of 24.
- The restor3d Outcomes RegistryNot yet recruitingNCT07563803
- Prospective Evaluation of Clinical and Radiographic Outcomes Following Total Talus Replacement (PROCLAIM)Enrolling by invitationNCT06311331
- A Multicenter Study to Evaluate Functional Outcome After Knee ReplacementTerminatedNCT02494544Not applicable
- A Prospective Study to Evaluate the iTotal Knee and iPoly XE Tibial InsertsTerminatedNCT03289754Not applicable
- Cervical Interbody Fusion Device Patient RegistryTerminatedNCT05114356
- Retrospective Evaluation of Clinical and Radiographic Outcomes Following Total Talus ReplacementCompletedNCT05231304
- A Prospective Study to Evaluate the ConforMIS iTotal® (PS) Knee Replacement SystemTerminatedNCT03152162
- iUni G2+ Prospective StudyTerminatedNCT01820676
- A Study to Evaluate the Conformis Hip SystemTerminatedNCT03738462
- A Retrospective Study to Evaluate the ConforMIS iUni, iDuo & iTotal® KRSCompletedNCT03152357
- Comparison of Knee Kinematics for Subjects Implanted With Either a ConforMIS or Traditional Knee ImplantCompletedNCT01717001
- A Single Time-Point Study to Evaluate the ConforMIS iTotal® (CR) Knee Versus Off-the-ShelfCompletedNCT02251522
- Study of the ConforMIS iDuo(R) G2TerminatedNCT01564641
- Costs and Benefits of ConforMIS iTotal® Knee Replacement System Versus Standard Total KneeCompletedNCT01899417
- A Single Time-Point Study to Evaluate the ConforMIS iTotal (PS) Knee Replacement System Versus Off-the-ShelfTerminatedNCT03146819
- Total Knee Arthroplasty Functional Outcomes Study Research DesignTerminatedNCT02228538
- TKA Operating Room Efficiency for TKA Using Customized Implant TechniquesTerminatedNCT04180423
- A Prospective, Multicenter Study to Evaluate the ConforMIS iTotal® (CR) Knee Replacement SystemTerminatedNCT01820650
- A Study to Evaluate the Conformis iTotal Identity Knee Replacement SystemTerminatedNCT04667559
- A Retrospective Study to Evaluate the ConforMIS iTotal® Posterior Stabilized (PS) Knee Replacement SystemCompletedNCT03289000
- A Retrospective Study of the iTotal CR Knee Replacement SystemCompletedNCT01564654
- In Vivo Comparison of Knee Kinematics for Subjects Implanted With Either a ConforMIS or Traditional Knee ImplantCompletedNCT01882751
- Study Comparing Fit of the iTotal Versus Standard Total Knee ImplantsTerminatedNCT01861028
- Multi-Center Study to Evaluate the ConforMIS iUni Knee ImplantTerminatedNCT01117571