Condition

Traumatic Arthritis

ClinicalTrials.gov condition label

Clinical trials37
Recruiting4
Common interventions25
Lead sponsors shown10

Clinical trials

37 shown
EMPHASYS Cup Positioning in THA With Non-Invasive Navigation (Velys Hip Navigation (VHN))NCT06631638 · 2025-10-24
RECRUITING
Post Market Clinical Follow-Up KeriFlex®NCT06546345 · 2023-11-14
RECRUITING
Physica System Total Knee Replacement Registry StudyNCT03048201 · 2017-03-24
RECRUITING
The Medacta International SMS Post-Marketing Surveillance StudyNCT02748408 · 2015-07-01
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
Tornier HRS (Humeral Reconstruction System) Study (REVIVE)NCT05500066 · 2023-01-11
ENROLLING_BY_INVITATION
The Medacta Quadra-P Anteverted StudyNCT05460715 · 2021-07-30
ACTIVE_NOT_RECRUITING
Persona Ti-Nidium Post-Market Clinical Follow-upNCT04817969 · 2021-06-01
ACTIVE_NOT_RECRUITING
The Medacta International GMK Sphere Cementless Post-Marketing Surveillance StudyNCT05003414 · 2020-01-14
ACTIVE_NOT_RECRUITING
The Medacta International AMIStem-P Post-Marketing Surveillance StudyNCT04997005 · 2019-04-26
ACTIVE_NOT_RECRUITING
Prospective Study for the Evaluation of the Cementless Anatomic Femoral Stem Minimax -LaunayNCT06012656 · 2019-01-02
ACTIVE_NOT_RECRUITING
Persona TM Tibia Clinical Outcomes StudyNCT03589300 · 2018-04-30
COMPLETED
NexGen TM Tibia Clinical Outcomes StudyNCT03272373 · 2017-10-03
COMPLETED
Long Term Follow-up of Integra® Cadence™ Total Ankle System in Primary Ankle Joint ReplacementNCT03247023 · 2017-09-18
TERMINATED
Clinical Evaluation of the Integra® Titan™ Modular Shoulder System Generation 2.5 for Primary Shoulder Joint ReplacementNCT03250767 · 2017-08-01
TERMINATED
Actis Total Hip System 2 Year Follow-upNCT02783274 · 2016-07-01
COMPLETED
Randomized Controlled Clinical Outcomes of the Vanguard XP Bicruciate Knee SystemNCT02175576 · 2014-10-01
TERMINATED
Persona Total Knee Arthroplasty Outcomes StudyNCT02255383 · 2014-07-01
ACTIVE_NOT_RECRUITING
Zimmer POLAR Persona - TKA (EMEA Study)NCT02337244 · 2013-11-18
ACTIVE_NOT_RECRUITING
Zimmer POLAR - Total Knee Arthroplasty (TKA)NCT01859130 · 2013-10-21
COMPLETED
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
The Medacta International GMK Sphere Post-Marketing Surveillance StudyNCT02199600 · 2012-10-01
ACTIVE_NOT_RECRUITING
A Prospective Munti-center Study on VANGUARD™ PS Total Knee Replacement SystemNCT01906177 · 2012-07-01
COMPLETED
A Clinical Evaluation of Metal Ion Release From Metal-on-Metal Cementless Total Hip ArthroplastyNCT00757354 · 2012-06-01
COMPLETED
A Prospective, Clinical Investigation of the Vanguard 360 Revision KneeNCT01542580 · 2012-03-01
ACTIVE_NOT_RECRUITING
Randomized Controlled Clinical Evaluation to Compare Vanguard Cruciate Retaining and AGC Total Condylar Knee ImplantsNCT01064063 · 2011-02-15
COMPLETED
Vanguard Rocc Post Market SurveillanceNCT03664791 · 2009-10-23
UNKNOWN
Vanguard Complete Knee Versus Vanguard High Flex Rotating Platform (RP) Knee StudyNCT01010269 · 2009-10-01
COMPLETED
Post-Market Study of the 3DKnee™ SystemNCT00819481 · 2009-02-01
COMPLETED
LPS Flex Porous Femoral ComponentsNCT01462240 · 2008-05-20
WITHDRAWN
3DKnee™ System vs. the MJS Knee SystemNCT00764803 · 2008-01-01
TERMINATED
A Clinical Investigation of Recovery Following Hip Resurfacing or Total Hip ArthroplastyNCT00585988 · 2007-06-01
WITHDRAWN
Total Knee Replacement Using Simplex® or Cobalt™ Bone CementNCT00589485 · 2006-11-01
WITHDRAWN
Maxim® Knee Pop-Top® Tibia vs. Regular Maxim® Knee TibiaNCT00579059 · 2004-05-01
TERMINATED
A Clinical Investigation of the Vanguard™ Complete Knee SystemNCT00698854 · 2004-03-01
COMPLETED

Common interventions

Zimmer Persona Total Knee SystemDEVICE33DKnee™ SystemDEVICE1Actis Total Hip SystemDEVICE1AGC kneeDEVICE1AMIStem-PDEVICE1Cemented Persona Knee SystemDEVICE1Cementless Persona Knee SystemDEVICE1Cobalt™ Bone CementDEVICE1E1-Hip BearingDEVICE1EMPHASYS Cup with VHNDEVICE1Encore 3DKnee™ systemDEVICE1Encore MJS™ Knee SystemDEVICE1GMK Sphere cementless Knee ReplacementDEVICE1GMK Sphere Knee ReplacementDEVICE1Hip Resurfacing SystemDEVICE1Implantation of Integra Cadence Total Ankle SystemDEVICE1Integra Titan Modular Shoulder System 2.5DEVICE1KeriFlex®DEVICE1LPS Flex Porous Femoral ComponentsDEVICE1M2a-Magnum™ Large Metal ArticulationDEVICE1Maxim® Knee System with Removable Molded Polyethylene TibiaDEVICE1Metal on Metal cementless hipPROCEDURE1MiniMAXDEVICE1NexGen TM Modular TibiaDEVICE1NexGen TM Monoblock TibiaDEVICE1

Trial status mix

ACTIVE_NOT_RECRUITING11
COMPLETED11
TERMINATED6
RECRUITING4
WITHDRAWN3
ENROLLING_BY_INVITATION1
UNKNOWN1

Phase mix

NA17

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