Condition

Avascular Necrosis

ClinicalTrials.gov condition label

Clinical trials78
Recruiting3
Common interventions25
Lead sponsors shown15

Clinical trials

60 shown
Post-Market Clinical Follow-Up (PMCF) Study Evaluating the Safety and Efficacy of Tıpmed™ Shoulder Prosthesis SystemNCT07678034 · 2025-06-16
RECRUITING
Clinical and Radiological Outcomes of Medacta Shoulder System FRNCT05926622 · 2022-03-15
RECRUITING
Physica System Total Knee Replacement Registry StudyNCT03048201 · 2017-03-24
RECRUITING
Post Market Clinical Follow-Up Study for EVOLUTION® NitrX™ Keeled Tibia and EVOLUTION® NitrX™ CS/CR Femur With Cruciate Sacrificing InsertNCT07391592 · 2025-08-18
ACTIVE_NOT_RECRUITING
Cemented vs Cementless Persona Keel RCTNCT05630053 · 2023-07-25
ACTIVE_NOT_RECRUITING
Persona OsseoTi Keel Compatibility Study (Total Knee Arthroplasty)NCT05787821 · 2023-06-28
ACTIVE_NOT_RECRUITING
G7 Freedom Constrained Vivacit-E LinersNCT05587244 · 2023-05-08
ENROLLING_BY_INVITATION
G7 Dual Mobility With Vivacit-E or Longevity PMCFNCT05548972 · 2023-03-20
ENROLLING_BY_INVITATION
Tornier HRS (Humeral Reconstruction System) Study (REVIVE)NCT05500066 · 2023-01-11
ENROLLING_BY_INVITATION
S-11 SMR TT Hybrid Glenoid and Cementless Finned Short StemNCT05314387 · 2022-04-01
NOT_YET_RECRUITING
Insignia™ Hip Stem Outcomes StudyNCT05144191 · 2022-02-07
ACTIVE_NOT_RECRUITING
TESS V3 Modular Total Shoulder System PMCFNCT05002959 · 2022-02-01
TERMINATED
Impact of a POPOP on Preoperative Health, Eligibility, and Clinical & Patient-Reported Outcomes in TJANCT04910048 · 2022-01-17
COMPLETED
Persona Ti-Nidium Post-Market Clinical Follow-upNCT04817969 · 2021-06-01
ACTIVE_NOT_RECRUITING
Clinical and Radiological Outcomes of Medacta Shoulder System (BE)NCT05002335 · 2020-10-06
ACTIVE_NOT_RECRUITING
Post Market Clinical Follow-Up Study for EVOLUTION® BIOFOAM® Tibia and EVOLUTION® CS/CR Porous FemurNCT04301622 · 2020-02-03
ACTIVE_NOT_RECRUITING
The Medacta International GMK Sphere Cementless Post-Marketing Surveillance StudyNCT05003414 · 2020-01-14
ACTIVE_NOT_RECRUITING
Prospective Study for the Evaluation of the Cementless Anatomic Femoral Stem Minimax -LaunayNCT06012656 · 2019-01-02
ACTIVE_NOT_RECRUITING
Clinical and Radiological Outcomes of Medacta Shoulder SystemNCT03547947 · 2018-06-13
ACTIVE_NOT_RECRUITING
G7 BiSpherical Acetabular Shell PMCF StudyNCT03266874 · 2017-12-10
ACTIVE_NOT_RECRUITING
Anatomical Shoulder Domelock System StudyNCT03312465 · 2017-09-28
ACTIVE_NOT_RECRUITING
AL-2 MP-1 (Polyimide) Acetabular LinerNCT02503891 · 2017-09-15
UNKNOWN
Randomized Controlled RSA Study Comparing the Taperloc Complete Versus the Taperloc Complete Microplasty.NCT03409666 · 2017-05-12
COMPLETED
Clinical Evaluation of the TITAN™ Total Shoulder SystemNCT03245320 · 2017-03-20
TERMINATED
BC Study of G7 Cup and Compatible Femoral StemsNCT03456622 · 2015-11-01
ACTIVE_NOT_RECRUITING
A Clinical Trial Study of Hip System in Primary Total Hip Arthroplasty in ChinaNCT02399007 · 2015-06-07
COMPLETED
Project JAY THA Registration StudyNCT02347384 · 2015-04-20
COMPLETED
Effects of Lacosamide on Post-operative Opioid Requirements After a Total Hip Arthroplasty:NCT02342977 · 2014-11-01
WITHDRAWN
Signature Acetabular Posterior/Lateral Data CollectionNCT02220478 · 2014-11-01
TERMINATED
TC-A Registration StudyNCT02139345 · 2014-09-23
COMPLETED
Comprehensive Nano - Post Market Clinical Follow-Up StudyNCT03423953 · 2013-10-30
ACTIVE_NOT_RECRUITING
Taperloc Complete Microplasty vs Taperloc Complete Standard: Randomized Controlled Study on Bone Mineral DensityNCT02087436 · 2013-03-01
COMPLETED
Evaluate E1 Wear, Clinical Performance of E1 Liner in THA in Korean Patient PopulationNCT02087449 · 2013-02-01
TERMINATED
Arcos Revision Stem: Evaluation of Clinical PerformanceNCT01820611 · 2013-02-01
COMPLETED
PMCF Study on the Safety and Performance of the Zimmer® Maxera™ Acetabular System in Total Hip ArthroplastyNCT03372278 · 2013-01-01
ACTIVE_NOT_RECRUITING
Trinity™ BIOLOX Delta™ CoC THR Multi-center StudyNCT01921309 · 2012-12-01
UNKNOWN
The Medacta International GMK Sphere Post-Marketing Surveillance StudyNCT02199600 · 2012-10-01
ACTIVE_NOT_RECRUITING
Sidus(TM) Post Market Clinical Follow-up (PMCF) StudyNCT01700543 · 2012-10-01
COMPLETED
Multi-centre Study to Assess the Long-term Performance of the Deltamotion Cup System in Primary Hip Replacement SurgeryNCT01635166 · 2012-07-01
TERMINATED
A Clinical Evaluation of Metal Ion Release From Metal-on-Metal Cementless Total Hip ArthroplastyNCT00757354 · 2012-06-01
COMPLETED
Metal Ions in Ceramic on Metal Total Hip ArthroplastyNCT01437124 · 2011-10-01
COMPLETED
Zimmer Continuum Metal on Polyethylene (MoP) PostMarket Clinical Followup (PMCF) StudyNCT01307384 · 2011-03-29
COMPLETED
Database Retrieval for the Comprehensive ShoulderNCT03409718 · 2011-02-24
ACTIVE_NOT_RECRUITING
PMCF Study of the CLS Brevius Stem With Kinectiv TechnologyNCT03410940 · 2011-01-07
TERMINATED
Outcomes Study of the TM Humeral Stem Used in Primary, Total or Hemi Shoulder ArthroplastyNCT01480453 · 2011-01-02
TERMINATED
Acetabular Shell Positioning Using Patient Specific InstrumentsNCT01791738 · 2011-01-01
COMPLETED
Outcomes Study of the Trabecular Metal (TM) Reverse Shoulder SystemNCT01480440 · 2011-01-01
ACTIVE_NOT_RECRUITING
Multi Centre Study on TESS V2 Shoulder SystemNCT03431857 · 2010-10-20
COMPLETED
An Electronic Data Capture Study to Assess the Long-term Performance of the DePuy PROXIMA™ Hip in Primary Total Hip ReplacementNCT01134445 · 2010-02-01
TERMINATED
Post-market Surveillance Study With the HYPERION Hip Endoprosthesis System in Defect ReconstructionNCT03382665 · 2010-01-01
TERMINATED
Post-PMA Approval Study: 10 Year Follow-Up IDE SubjectsNCT00721994 · 2008-05-01
COMPLETED
Cormet Post-PMA Study: New EnrollmentNCT00722007 · 2008-04-24
COMPLETED
Fitmore Hip Stem PMCF Study: A Multi-centre, Non-comparative, Prospective Post-market Clinical Follow-up Study.NCT03411044 · 2008-02-08
COMPLETED
Efficacy of the CLP® Hip - RetrospectiveNCT00764842 · 2008-01-01
TERMINATED
Retrospective Study of the Linear™ HipNCT00764959 · 2007-10-01
TERMINATED
A Clinical Investigation of the Comprehensive®, BioModular®, and Bi-Angular® Shoulder SystemsNCT00699270 · 2007-08-01
WITHDRAWN
Metal on Metal Versus Metal on Highly Crossed Linked Polyethylene SytemNCT01422564 · 2007-01-01
TERMINATED
A Single Centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Ceramic-on-ceramic Bearing in Primary Total Hip ReplacementNCT00872222 · 2007-01-01
TERMINATED
The 3DKnee™ System: A Post-Market StudyNCT00764673 · 2006-10-01
COMPLETED
Multi-Centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Resurfacing and Primary Total Hip ReplacementNCT00872547 · 2006-09-01
TERMINATED

Common interventions

DePuy ASR™ Hip SystemDEVICE2DePuy Proxima™ HipDEVICE2Medacta Shoulder SystemDEVICE2Total Knee ArthroplastyDEVICE23DKneeDEVICE1Acetabular cupDEVICE1Acetabular positioning systemPROCEDURE1Alumina/AluminaDEVICE1Anatomic TESS V3DEVICE1Arcos Revision Stem SystemDEVICE1AS Domelock SystemDEVICE1BIOLOX forte ball head + SL-PLUS StemDEVICE1Biomet Comprehensive Shoulder SystemDEVICE1C-Stem™ AMT Femoral Component (standard and high off-set variants)DEVICE1Cemented Persona Knee SystemDEVICE1Cementless Persona Knee SystemDEVICE1CLS Brevius stem with Kinectiv technologyDEVICE1coated femoral hip stemDEVICE1Comprehensive NanoDEVICE1Continuum Metal on Polyethylene Acetabular SystemDEVICE1Cormet Hip ResurfacingDEVICE1Cormet Hip Resurfacing SystemDEVICE1Delta MotionDEVICE1Delta PLUS Femoral Head + SL-TWIN StemDEVICE1DePuy ASR Hip SystemDEVICE1

Trial status mix

COMPLETED25
TERMINATED23
ACTIVE_NOT_RECRUITING18
ENROLLING_BY_INVITATION3
RECRUITING3
WITHDRAWN3
UNKNOWN2
NOT_YET_RECRUITING1

Phase mix

NA23
PHASE414
PHASE11
PHASE21

Registry-derived research relationships: ClinicalTrials.gov. Raw condition and intervention labels remain distinct from canonical MONDO/RxNorm entities unless separately normalized.