Zimmer Biomet: all 312 studies
Page 3 of 4. Open to participants first (30), then studies with results posted, then the rest; newest registration first within each.
- Biologically Assisted Core Decompression of the Femoral Head Using the PerFuse Instrument and BioCUEStatus unknownNCT02662881
- BOLD MRI as a Surrogate of Improved Muscle Oxygenation Following Endovascular Therapy for the Treatment of CLICompletedNCT02601430Not applicable
- Recover L-PRP in Lateral Epicondylitis (REGP-11-00)TerminatedNCT02588040
- Prospective Post-Market Data Collection on Patients With Knee OA and Treated With nSTRIDE APSCompletedNCT02580643
- A 3-Arm Study on G7 Acetabular Cup With Echo BiMetric Stem in Total Hip ArthroplastyActive, not recruitingNCT02518269Not applicable
- Zimmer CAS PSI X-Ray Knee in TKA (Total Knee Arthroplasty)CompletedNCT02504112
- Safety and Efficacy of Autologous Concentrated Bone Marrow Aspirate for Critical Limb Ischemia - Continued AccessNo longer availableNCT02474121
- Hydroxyapatite (HA) Coating Versus Plasma Porous Spray (PPS) in Press-fit Acetabular Components Early Outcomes With DEXACompletedNCT02447653Not applicable
- Post-Market Surveillance Study of the TM Ardis Interbody Fusion SystemCompletedNCT02429908Phase 4
- Multicentre Prospective Study to Evaluate Long-term Clinical Outcomes of the Sirius Cemented Femoral StemActive, not recruitingNCT02371382
- Cementless Oxford Partial Knee Controlled Observational StudyCompletedNCT02350049
- G7 Acetabular System vs. Exceed ABT Acetabular System in THACompletedNCT02340390Not applicable
- Zimmer POLAR Persona - TKA (EMEA Study)Active, not recruitingNCT02337244
- Investigation to Determine Safety of Taperloc Stems With BioGuard Coating When Used in Cementless Total Hip ArthroplastyActive, not recruitingNCT02263209Not applicable
- Persona Total Knee Arthroplasty Outcomes StudyActive, not recruitingNCT02255383Not applicable
- Enhanced Metal Reduction Techniques for Definitive CT Scanning to Assess Spinal Fusion With TM-ArdisWithdrawnNCT02170558
- Prospective Multi-Center Study on Vanguard With E1 BearingTerminatedNCT02088372
- Evaluate E1 Wear, Clinical Performance of E1 Liner in THA in Korean Patient PopulationTerminatedNCT02087449
- Taperloc Complete Microplasty vs Taperloc Complete Standard: Randomized Controlled Study on Bone Mineral DensityCompletedNCT02087436Not applicable
- COMPREHENSIVE® REVERSE SHOULDER Mini BasePlateCompletedNCT02084693
- Zimmer Trabecular Metal Total Ankle PMCFActive, not recruitingNCT02038140Not applicable
- A Prospective Munti-center Study on VANGUARD™ PS Total Knee Replacement SystemCompletedNCT01906177
- Sidus(TM) Post Market Clinical Follow-up (PMCF) StudyCompletedNCT01700543
- DeNovo NT Natural Tissue Graft Stratified Knee StudyStatus unknownNCT01670617Not applicable
- Evaluation of Subchondroplasty™ for Defects Associated With Bone Marrow LesionsCompletedNCT01621893
- Aspen Spinous Process Fixation System for Use in PLF in Patients With SpondylolisthesisTerminatedNCT01560273
- Comparison of the Aspen Device Versus Pedicle Screws for Supplemental Posterior Fixation in Lumbar Interbody FusionCompletedNCT01549366Not applicable
- A Prospective, Clinical Investigation of the Vanguard 360 Revision KneeActive, not recruitingNCT01542580
- Outcomes Study of the TM Humeral Stem Used in Primary, Total or Hemi Shoulder ArthroplastyTerminatedNCT01480453
- Outcomes Study of the Trabecular Metal (TM) Reverse Shoulder SystemActive, not recruitingNCT01480440
- Patello-Femoral Joint Post Market Clinical Follow-up Within the Knee RegistryWithdrawnNCT01469806
- Gender Solutions Natural Knee Post-Market StudyWithdrawnNCT01463566
- LPS Flex Porous Femoral ComponentsWithdrawnNCT01462240
- Oxford Partial Knee Comparative Instrument Pilot StudyCompletedNCT01410786Not applicable
- Chondrofix Osteochondral Allograft Prospective StudyTerminatedNCT01410136Not applicable
- DeNovo NT Ankle LDC StudyStatus unknownNCT01347892
- DeNovo NT Longitudinal Data Collection (LDC) Knee StudyStatus unknownNCT01329445
- 10 Year Clinical Evaluation of Primoris Hip ComponentActive, not recruitingNCT01326832
- Vanguard Knee Anterior Stabilized Versus Posterior Stabilized Bearing StudyWithdrawnNCT01308515Not applicable
- Zimmer Continuum Metal on Polyethylene (MoP) PostMarket Clinical Followup (PMCF) StudyCompletedNCT01307384
- Signature Versus Computer Assisted Surgery StudyCompletedNCT01256216Not applicable
- A Multicentre Trial to Compare Two Articulating Bearing Surfaces as Used in Cementless Primary Hip ArthroplastyTerminatedNCT01247038Not applicable
- Post Market Surveillance to Evaluate the Effectiveness the Polaris Deformity Spinal SystemCompletedNCT01220505
- A Comparison Between Signature Total Knee Arthroplasty (TKA) to Conventional TKA and Computer Assisted TKACompletedNCT01145157Not applicable
- ChonDux for Filling Full Thickness Cartilage Defects in the Femoral Condyle of the KneeTerminatedNCT01110070Not applicable
- Short-Term Clinical Outcome of Total Hip Arthroplasty Using Larger Diameter of 4th Generation Ceramic BearingCompletedNCT01103882
- Signature Personalised Patient Care System With the Vanguard Knee System StudyTerminatedNCT01092312Not applicable
- Randomized Controlled Clinical Evaluation to Compare Vanguard Cruciate Retaining and AGC Total Condylar Knee ImplantsCompletedNCT01064063Not applicable
- Feasibility Study of Anti-inflammatory Cytokines in Whole Blood in Osteoarthritis PatientsCompletedNCT01050894
- Efficacy of the Aspen Spinous Process System in Anterior Lumbar Interbody Fusion (ALIF)WithdrawnNCT01016314Not applicable
- Review on Minimally Invasive Skin Incision in Vanguard PS Artificial Knee Joint SystemCompletedNCT01010828Not applicable
- Vanguard Complete Knee Versus Vanguard High Flex Rotating Platform (RP) Knee StudyCompletedNCT01010269Not applicable
- Oxford Unicompartmental Knee Arthroplasty With and Without Navigational UnitCompletedNCT00862316Not applicable
- Regenerex Tibial Tray Multi-Center Data CollectionCompletedNCT00859963
- Pro Osteon Bone Void Filler StudyWithdrawnNCT00858598
- Avascular Necrosis (AVN) Long-Term Follow-upTerminatedNCT00833430
- MIS MiLIF Versus OpenCompletedNCT00792129
- Post Market Study of DeNovo NT, Natural Tissue GraftCompletedNCT00791245
- Posterior Lateral Fusion (PLF) With DynesysCompletedNCT00791180
- CopiOs(TM) Bone Void Filler in the Post-Harvest Iliac CrestCompletedNCT00768924
- A Prospective Randomized Study on Vanguard Cruciate Retaining Versus Vanguard High Flex Posterior Stabilized Total Knee System in the Early Range of MotionCompletedNCT00763113Not applicable
- Total Temporomandibular Joint Replacement System Post Approval StudyCompletedNCT00762944
- The Value of Platelet-Rich Plasma in Chronic Midportion Achilles Tendinopathy: a Double-blind Randomized Clinical TrialCompletedNCT00761423Phase 4
- Retrospective Study on Cenos Stem With BoneMaster HAWithdrawnNCT00761046
- Prospective Data Collection on Cementless Oxford Partial KneeWithdrawnNCT00760188
- Outcome Analysis of the Oxford Partial Knee ArthroplastyCompletedNCT00759616Not applicable
- A Clinical Study of the Dynesys(R) Spinal SystemTerminatedNCT00759057Phase 3
- ROCC Knee Data CollectionTerminatedNCT00758901
- Evaluate Effectiveness of the Biomet Lumbar Spinal Fusion SystemCompletedNCT00758719
- Platelet Rich Plasma to Treat Plantar FasciitisCompletedNCT00758641Phase 4
- ReCap Total Hip Resurfacing Prospective Data CollectionTerminatedNCT00758472
- Data Collection on ReCap/Magnum in Total Hip Replacement and ResurfacingCompletedNCT00758355
- Retrospective Data Review of ReCap Total Hip ResurfacingWithdrawnNCT00758329
- Retrieval Study and Histological Examination Of A Hip Femoral Components With Hydroxyapatite CoatingsTerminatedNCT00757653Not applicable
- A Clinical Evaluation of Metal Ion Release From Metal-on-Metal Cementless Total Hip ArthroplastyCompletedNCT00757354Not applicable
- Platelet-rich-plasma Treating Tennis ElbowCompletedNCT00757289Not applicable
- Clinical Evaluation on HA Coated Dynamic Hip Screws for Trochanteric Femoral FracturesWithdrawnNCT00756431Not applicable
- A Randomized Control Trial to Assess Early Clinical and Functional Outcome of the ROCC and LCS Total Knee Implant DesignsCompletedNCT00755144Not applicable
- Clinical Study on BiHapro Total Hip System With Different Surface CoatingsTerminatedNCT00755001
- Microplasty Tibial Tray Data CollectionWithdrawnNCT00754637
- S.E.S Shoulder Arthroplasty Data CollectionTerminatedNCT00754416
- TESS Shoulder Arthroplasty Data CollectionTerminatedNCT00751673
- A Comparison of Two Different Surgical Techniques for Total Hip ResurfacingCompletedNCT00750984Not applicable
- Durom(R) Hip Resurfacing System Multicenter TrialCompletedNCT00746616Phase 3
- Evaluation Of Spinelink® Fixation In The Treatment Of Degenerative Spondylolisthesis And Spinal InstabilityCompletedNCT00726310
- Spine Patient Outcomes Registry for Biomet/EBI (Electro-Biology, Inc)CompletedNCT00726284
- Study to Analyze the Effects of EBI OsteoGen™ on the Surgical Reconstruction of Tibia Non-unionsTerminatedNCT00726193
- Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate SystemCompletedNCT00726128
- Pediatric Locking Nail for the Treatment of Femoral Fractures in ChildrenCompletedNCT00725894
- OsseoFit™ Prospective Data CollectionWithdrawnNCT00708474Not applicable
- A Clinical Investigation of the Taperloc® Microplasty™ Hip SystemCompletedNCT00699309
- A Clinical Investigation of the Comprehensive®, BioModular®, and Bi-Angular® Shoulder SystemsWithdrawnNCT00699270
- A Clinical Investigation of the Oxford® Partial Knee SystemTerminatedNCT00699257
- A Clinical Investigation of the Balance® Microplasty™ Hip SystemCompletedNCT00699088
- A Clinical Investigation of the Vanguard™ Complete Knee SystemCompletedNCT00698854
- A Clinical Investigation of the Copeland™ Humeral Resurfacing HeadTerminatedNCT00698750
- A Clinical Investigation of the M2a- Taper™ Hip SystemTerminatedNCT00698633
- A Clinical Investigation of the M2a- 38™ Hip SystemTerminatedNCT00698503
- A Clinical Investigation of the M2a-Magnum™ Hip SystemTerminatedNCT00698347
- A Clinical Investigation of ArComXL® Polyethylene in Total Hip ReplacementCompletedNCT00698152