Condition

Avascular Necrosis

ClinicalTrials.gov condition label

How to interpret these research links

Connected source records

This is the original ClinicalTrials.gov condition label, found in 78 distinct published trials. It is kept separate from a MONDO disease identifier until a specific normalization is supported. Related interventions are co-recorded in studies; they are not medical recommendations.

Data basis: current published ClinicalTrials.gov records and, where present, RxNorm, MONDO and FDA-label identifiers. See the evidence interpretation and counting methodology.

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

Clinical and Radiological Outcomes of Medacta Shoulder System FRNCT05926622 · 2022-03-15

Physica System Total Knee Replacement Registry StudyNCT03048201 · 2017-03-24

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

Impact of a POPOP on Preoperative Health, Eligibility, and Clinical & Patient-Reported Outcomes in TJANCT04910048 · 2022-01-17

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

Randomized Controlled RSA Study Comparing the Taperloc Complete Versus the Taperloc Complete Microplasty.NCT03409666 · 2017-05-12

Clinical Evaluation of the TITAN™ Total Shoulder SystemNCT03245320 · 2017-03-20

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

Project JAY THA Registration StudyNCT02347384 · 2015-04-20

Effects of Lacosamide on Post-operative Opioid Requirements After a Total Hip Arthroplasty:NCT02342977 · 2014-11-01

Signature Acetabular Posterior/Lateral Data CollectionNCT02220478 · 2014-11-01

TC-A Registration StudyNCT02139345 · 2014-09-23

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

Evaluate E1 Wear, Clinical Performance of E1 Liner in THA in Korean Patient PopulationNCT02087449 · 2013-02-01

Arcos Revision Stem: Evaluation of Clinical PerformanceNCT01820611 · 2013-02-01

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

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

Multi-centre Study to Assess the Long-term Performance of the Deltamotion Cup System in Primary Hip Replacement SurgeryNCT01635166 · 2012-07-01

A Clinical Evaluation of Metal Ion Release From Metal-on-Metal Cementless Total Hip ArthroplastyNCT00757354 · 2012-06-01

Metal Ions in Ceramic on Metal Total Hip ArthroplastyNCT01437124 · 2011-10-01

Zimmer Continuum Metal on Polyethylene (MoP) PostMarket Clinical Followup (PMCF) StudyNCT01307384 · 2011-03-29

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

Outcomes Study of the TM Humeral Stem Used in Primary, Total or Hemi Shoulder ArthroplastyNCT01480453 · 2011-01-02

Acetabular Shell Positioning Using Patient Specific InstrumentsNCT01791738 · 2011-01-01

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

An Electronic Data Capture Study to Assess the Long-term Performance of the DePuy PROXIMA™ Hip in Primary Total Hip ReplacementNCT01134445 · 2010-02-01

Post-market Surveillance Study With the HYPERION Hip Endoprosthesis System in Defect ReconstructionNCT03382665 · 2010-01-01

Post-PMA Approval Study: 10 Year Follow-Up IDE SubjectsNCT00721994 · 2008-05-01

Cormet Post-PMA Study: New EnrollmentNCT00722007 · 2008-04-24

Fitmore Hip Stem PMCF Study: A Multi-centre, Non-comparative, Prospective Post-market Clinical Follow-up Study.NCT03411044 · 2008-02-08

Efficacy of the CLP® Hip - RetrospectiveNCT00764842 · 2008-01-01

Retrospective Study of the Linear™ HipNCT00764959 · 2007-10-01

A Clinical Investigation of the Comprehensive®, BioModular®, and Bi-Angular® Shoulder SystemsNCT00699270 · 2007-08-01

Metal on Metal Versus Metal on Highly Crossed Linked Polyethylene SytemNCT01422564 · 2007-01-01

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

The 3DKnee™ System: A Post-Market StudyNCT00764673 · 2006-10-01

Multi-Centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Resurfacing and Primary Total Hip ReplacementNCT00872547 · 2006-09-01

Common interventions

DePuy ASR™ Hip SystemDEVICE2 DePuy Proxima™ HipDEVICE2 Medacta Shoulder SystemDEVICE2 Total Knee ArthroplastyDEVICE2 3DKneeDEVICE1 Acetabular cupDEVICE1 Acetabular positioning systemPROCEDURE1 Alumina/AluminaDEVICE1 Anatomic TESS V3DEVICE1 Arcos Revision Stem SystemDEVICE1 AS Domelock SystemDEVICE1 BIOLOX forte ball head + SL-PLUS StemDEVICE1 Biomet Comprehensive Shoulder SystemDEVICE1 C-Stem™ AMT Femoral Component (standard and high off-set variants)DEVICE1 Cemented Persona Knee SystemDEVICE1 Cementless Persona Knee SystemDEVICE1 CLS Brevius stem with Kinectiv technologyDEVICE1 coated femoral hip stemDEVICE1 Comprehensive NanoDEVICE1 Continuum Metal on Polyethylene Acetabular SystemDEVICE1 Cormet Hip ResurfacingDEVICE1 Cormet Hip Resurfacing SystemDEVICE1 Delta MotionDEVICE1 Delta PLUS Femoral Head + SL-TWIN StemDEVICE1 DePuy ASR Hip SystemDEVICE1

Leading sponsors

Zimmer Biomet 27 DePuy International 12 Medacta International SA 6 Biomet Orthopedics, LLC 5 Corin 4 Encore Medical, L.P. 4 DePuy Orthopaedics 3 Limacorporate S.p.a 2 MicroPort Orthopedics Inc. 2 Hussain Kazi 1 Indiana University 1 Johnson & Johnson Medical (Suzhou) Ltd. 1 M.M.A Tech Ltd. 1 Nova Scotia Health Authority 1 Smith & Nephew Medical (Shanghai) Ltd 1

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.