MicroPort Scientific Corporation: Joint Diseases trials
The registry lists 22 Joint Diseases studies with MicroPort Scientific Corporation as lead sponsor. 5 are open to participants now and 0 have results posted.
No phase 22(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.
- EVOLUTION® Revision STEMMED CS Post Market Clinical Follow-up Study ProtocolRecruitingNCT06142669
- Post Market Clinical Follow-Up Study for EVOLUTION® NitrX™ Keeled Tibia and EVOLUTION® NitrX™ CS/CR Femur With Cruciate Sacrificing InsertEnrolling by invitationNCT04816773
- Post Market Clinical Follow-Up Study for PROFEMUR® Preserve Classic Femoral StemEnrolling by invitationNCT04147559
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Z Revision Femoral StemsEnrolling by invitationNCT04064008
- Post Market Clinical Follow-Up Study Protocol for PROCOTYL® C Acetabular ComponentsEnrolling by invitationNCT03576573
- Post Market Clinical Follow-Up Study for EVOLUTION® NitrX™ Keeled Tibia and EVOLUTION® NitrX™ CS/CR Femur With Cruciate Sacrificing InsertActive, not recruitingNCT07391592
- Post Market Clinical Follow-Up Study for MicroPort PROFEMUR® Preserve Classic Femoral StemWithdrawnNCT04615039
- Post Market Clinical Follow-Up Study for EVOLUTION® BIOFOAM® Tibia and EVOLUTION® CS/CR Porous FemurActive, not recruitingNCT04301622
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Preserve Femoral StemActive, not recruitingNCT03865667
- Evaluation of Bone Mineral Density Changes After Total Hip Replacement: A Two-Year Clinical and DXA AnalysisCompletedNCT02865447
- PMCF Study Protocol for PROFEMUR® Gladiator Plasma Femoral Stems and PROCOTYL® L Beaded Acetabular ComponentsActive, not recruitingNCT02823834
- Radiostereometric Analysis (RSA) of the PROFEMUR® Preserve Classic Femoral ComponentsWithdrawnNCT02668211Not applicable
- Gait and Functional Outcomes Study Following Total Knee Arthroplasty With Medial-pivot or Posterior-stabilized ImplantsCompletedNCT02589197
- PMCF Study for PROFEMUR® Am Femoral Components and PROCOTYL® O HA Coated Acetabular ComponentsWithdrawnNCT02507258
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Gladiator Cemented Femoral StemsTerminatedNCT02397746
- Post Market Follow-Up Study of the EVOLUTION® Total Knee Arthroplasty System With Cruciate Sacrificing InsertsActive, not recruitingNCT02351414
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® L Revision Femoral StemsActive, not recruitingNCT02314702
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Gladiator HA Coated Modular Femoral StemsTerminatedNCT02314611
- Post Market Clinical Follow-up Study Protocol for PROFEMUR® Xm Femoral StemsTerminatedNCT02309593
- Post Market Clinical Follow-Up Study Protocol for CONSERVE® Press-Fit Femoral ComponentsActive, not recruitingNCT02285842
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® TL Modular Femoral StemsActive, not recruitingNCT02239783
- Post Market Clinical Follow-up Study Protocol for DYNASTY® BioFoam® Acetabular ComponentsActive, not recruitingNCT02149667