Clinical Trials Directory

Trials / Conditions / Congenital Hip Dysplasia

Congenital Hip Dysplasia

41 registered clinical trials studyying Congenital Hip Dysplasia2 currently recruiting.

StatusTrialSponsorPhase
Active Not RecruitingA Multi-Centre Study in Patients Undergoing Total Hip Arthroplasty With the Smith+Nephew CATALYSTEM™ Primary H
NCT06564636
Smith & Nephew, Inc.
Active Not RecruitingThe Medacta Quadra-P Anteverted Study
NCT05460715
Medacta International SA
Active Not RecruitingException Cementless Hip Stem
NCT04349046
Zimmer Biomet
CompletedPelvic Osteotomy Of The Total Hip Replacement
NCT06209255
Van Bölge Eğitim ve Araştırma Hastanesi
CompletedPericapsular Nerve Group (PENG) Block for Congenital Hip Dislocation Surgery
NCT04212039
Ataturk UniversityN/A
Active Not RecruitingThe Medacta International AMIStem-P Post-Marketing Surveillance Study
NCT04997005
Medacta International SA
CompletedErector Spinae Plane Block for Congenital Hip Dislocation Surgery
NCT03949686
Ataturk UniversityN/A
Active Not RecruitingProspective Study for the Evaluation of the Cementless Anatomic Femoral Stem Minimax -Launay
NCT06012656
Medacta International SA
UnknownEarly Abduction Splintage on Stable Hips in Infants With Developmental Dysplasia of the Hip
NCT02885831
University Hospital, Brest
RecruitingGlobal Hip Dysplasia Registry
NCT04117685
University of British Columbia
CompletedActis Total Hip System 2 Year Follow-up
NCT02783274
DePuy OrthopaedicsN/A
Active Not RecruitingAvenir® Cemented Hip Stem - PMCF
NCT03396224
Zimmer Biomet
RecruitingThe Medacta International SMS Post-Marketing Surveillance Study
NCT02748408
Medacta International SA
CompletedA Clinical Trial Study of Hip System in Primary Total Hip Arthroplasty in China
NCT02399007
Johnson & Johnson Medical (Suzhou) Ltd.N/A
CompletedClinical and Radiographic Outcomes of the Corin Tri-Fit Total Hip Replacement
NCT02162186
Corin
Active Not RecruitingVivacit-E Post-market Follow-up Study
NCT03226808
Zimmer BiometN/A
TerminatedA Multi-centre, Prospective Surveillance to Assess Mid-term Performance of the Mpact Cup
NCT02196818
Medacta International SA
Active Not RecruitingPMCF Study on the Safety and Performance of the Zimmer® Maxera™ Acetabular System in Total Hip Arthroplasty
NCT03372278
Zimmer Biomet
TerminatedMulti-centre Study to Assess the Long-term Performance of the Deltamotion Cup System in Primary Hip Replacemen
NCT01635166
DePuy InternationalPhase 4
Active Not RecruitingAVANTAGE® RELOAD Double Mobility Acetabular Cup -Clinical Study
NCT03357445
Zimmer BiometN/A
CompletedPeriprosthetic Bone Mineral Density After Total Hip Arthroplasty Performed Through a Minimally Invasive Anteri
NCT01285843
Medacta International SAN/A
TerminatedAn Electronic Data Capture Study to Assess the Long-term Performance of the DePuy PROXIMA™ Hip in Primary Tota
NCT01134445
DePuy InternationalPhase 4
Active Not RecruitingAMIStem Primary Hip System Prospective Post-marketing Multi-centre Surveillance Study
NCT01107340
Medacta International SAN/A
TerminatedTrilogy AB Acetabular Hip System Post Approval Study
NCT00715026
Zimmer BiometPhase 4
CompletedEBIS: The Eindhoven Breech Intervention Study
NCT00516555
Catharina Ziekenhuis Eindhoven
TerminatedA Single Centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Ceramic-on-ceramic Beari
NCT00872222
DePuy InternationalPhase 4
TerminatedMulti-Centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Resurfacing and Primary Tot
NCT00872547
DePuy InternationalPhase 4
TerminatedA Two Centre Study to Assess the Stability and Long-term Performance of the C-Stem™ AMT in a Total Primary Hip
NCT00872573
DePuy InternationalPhase 4
TerminatedA Randomised Study to Compare Metal Ion Release and Long-term Performance of the Pinnacle™ Cup With a Ceramic-
NCT00873444
DePuy InternationalPhase 4
CompletedA Clinical Investigation of the C2a-Taper™ Acetabular System
NCT00578851
Biomet Orthopedics, LLC
CompletedA Study to Assess the Long-term Performance of SmartSet® HV and SmartSet® GHV Bone Cements in Primary Total Hi
NCT00872066
DePuy InternationalPhase 4
TerminatedPost-approval Study of the DURALOC® Option Ceramic-on-Ceramic Hip Prosthesis System
NCT00546598
DePuy OrthopaedicsPhase 4
TerminatedA Multi-centre Study to Assess the Long-term Performance of the DePuy PROXIMA™ Hip in Primary Total Hip Replac
NCT00208455
DePuy InternationalPhase 4
WithdrawnA Multi-centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Polyethylene-on-metal Bea
NCT00208429
DePuy InternationalPhase 4
TerminatedA Two Centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Metal-on-Metal Bearing in P
NCT00208364
DePuy InternationalPhase 4
TerminatedA Single Centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Primary Hip Resurfacing
NCT00872794
DePuy InternationalPhase 4
TerminatedA Multi-centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Primary Hip Resurfacing S
NCT00208377
DePuy InternationalPhase 4
TerminatedA Multi-centre Study to Assess the Long-term Performance of the Summit™ Hip in Primary Total Hip Replacement
NCT00208390
DePuy InternationalPhase 4
CompletedA Randomised Single Centre Study to Compare the Long-term Wear Characteristics of Marathon™ and Enduron™ Polye
NCT00208442
DePuy InternationalPhase 4
TerminatedA Randomised Multi-centre Study to Compare the Long-term Performance of the Future Hip to 3 Other Implants in
NCT00208468
DePuy InternationalPhase 3
TerminatedA Randomised Single Centre Study to Compare the Long-term Performance of 4 Designs of the DePuy Ultima LX Stem
NCT00208351
DePuy InternationalPhase 3