MicroPort Scientific Corporation: Osteonecrosis trials
The registry lists 15 Osteonecrosis studies with MicroPort Scientific Corporation as lead sponsor. 4 are open to participants now and 0 have results posted.
No phase 15(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.
- 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- EVOLUTION® Revision CCKEnrolling by invitationNCT04145401
- 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 EVOLUTION® BIOFOAM® Tibia and EVOLUTION® CS/CR Porous FemurActive, not recruitingNCT04301622
- PMCF Study Protocol for PROFEMUR® Gladiator Plasma Femoral Stems and PROCOTYL® L Beaded Acetabular ComponentsActive, not recruitingNCT02823834
- 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 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