44 studies found for:    "Developmental dysplasia of hip"
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Rank Status Study
21 Unknown  A Randomised Single Centre Study to Compare the Long-Term Wear Characteristics of Marathon™ and Enduron™ Polyethylene Cup Liners in Primary Total Hip Replacement
Conditions: Osteoarthritis;   Post-Traumatic Arthritis;   Collagen Disorders;   Avascular Necrosis;   Traumatic Femoral Fractures;   Nonunion of Femoral Fractures;   Congenital Hip Dysplasia;   Slipped Capital Femoral Epiphysis
Interventions: Device: Marathon™;   Device: Enduron
22 Unknown  Periprosthetic Bone Mineral Density After Total Hip Arthroplasty Performed Through a Minimally Invasive Anterior Approach (AMIS) With Either an AMIStem or a Quadra Femoral Component
Conditions: Osteoarthritis;   Arthritis;   Avascular Necrosis;   Fracture of the Femoral Neck or Head;   Congenital Hip Dysplasia
Intervention: Procedure: Anterior Minimally Invasive Approach (AMIS)
23 Terminated A Randomised Study to Compare Metal Ion Release and Long-term Performance of the Pinnacle™ Cup With a Ceramic-on-Metal or a Metal-on-Metal Bearing
Conditions: Osteoarthritis;   Post-traumatic Arthritis;   Collagen Disorders;   Avascular Necrosis;   Congenital Hip Dysplasia;   Slipped Capital Femoral Epiphysis
Intervention: Device: Pinnacle™ Acetabular System
24 Recruiting An Electronic Data Capture Study to Assess the Long-term Performance of the DePuy PROXIMA™ Hip in Primary Total Hip Replacement
Conditions: Rheumatoid Arthritis;   Osteoarthritis;   Post-traumatic Arthritis;   Avascular Necrosis;   Traumatic Femoral Fractures;   Congenital Hip Dysplasia
Intervention: Device: DePuy Proxima™ Hip
25 Active, not recruiting Multi-Centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Resurfacing and Primary Total Hip Replacement
Conditions: Rheumatoid Arthritis;   Osteoarthritis;   Post-traumatic Arthritis;   Collagen Disorders;   Avascular Necrosis;   Nonunion of Femoral Fractures;   Congenital Hip Dysplasia;   Slipped Capital Femoral Epiphysis
Interventions: Device: DePuy ASR™ Hip System;   Device: DePuy ASR™ XL Head / ASR™ Acetabular Cup System
26 Terminated A Randomised Single Centre Study to Compare the Long-term Performance of 4 Designs of the DePuy Ultima LX Stem in Primary Total Hip Replacement
Conditions: Osteoarthritis;   Post-traumatic Arthritis;   Collagen Disorder;   Avascular Necrosis;   Traumatic Femoral Fractures;   Nonunion of Femoral Fractures;   Congenital Hip Dysplasia;   Slipped Capital Femoral Epiphysis
Interventions: Device: Ultima LX Collared Stem - Blasted Finished;   Device: Ultima LX Collared Stem - Polished Finished;   Device: Ultima LX Collarless Stem - Blasted Finished;   Device: Ultima LX Collarless Stem - Polished finished
27 Active, not recruiting A Clinical Investigation of the C2a-Taper™ Acetabular System
Conditions: Osteoarthritis;   Avascular Necrosis;   Congenital Hip Dysplasia;   Traumatic Arthritis
Intervention: Device: C2a - Taper™ Acetabular System
28 Completed EBIS: The Eindhoven Breech Intervention Study
Conditions: Breech Presentation;   External Cephalic Version;   Thyroid Hormones;   Stress, Psychological;   Congenital Hip Dysplasia
Intervention:
29 Active, not recruiting A Two Centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Metal-on-Metal Bearing in Primary Total Hip Replacement
Conditions: Rheumatoid Arthritis;   Osteoarthritis;   Post-traumatic Arthritis;   Collagen Disorders;   Avascular Necrosis;   Traumatic Femoral Fractures;   Nonunion of Femoral Fractures;   Congenital Hip Dysplasia;   Slipped Capital Femoral Epiphysis
Intervention: Device: Pinnacle Acetabular Cup System
30 Active, not recruiting A Study to Assess the Long-term Performance of SmartSet® HV and SmartSet® GHV Bone Cements in Primary Total Hip Replacement
Conditions: Rheumatoid Arthritis;   Osteoarthritis;   Post-traumatic Arthritis;   Collagen Disorders;   Avascular Necrosis;   Traumatic Femoral Fractures;   Nonunion of Femoral Fractures;   Congenital Hip Dysplasia;   Slipped Capital Femoral Epiphysis
Interventions: Device: SmartSet® HV bone cement;   Device: SmartSet® GHV bone cement
31 Recruiting Multi-centre Study to Assess the Long-term Performance of the Deltamotion Cup System in Primary Hip Replacement Surgery
Conditions: Rheumatoid Arthritis;   Osteoarthritis;   Post-traumatic Arthritis;   Avascular Necrosis;   Traumatic Femoral Fractures;   Congenital Hip Dysplasia
Intervention: Device: Delta Motion
32 Terminated A Randomised Multi-centre Study to Compare the Long-term Performance of the Future Hip to 3 Other Implants in Primary Total Hip Replacement
Conditions: Osteoarthritis;   Post-traumatic Arthritis;   Collagen Disorders;   Avascular Necrosis;   Traumatic Femoral Fractures;   Nonunion of Femoral Fractures;   Congenital Hip Dysplasia;   Slipped Capital Femoral Epiphysis;   Perthes Disease
Interventions: Device: Future Hip;   Device: Omniflex;   Device: Zueymüller;   Device: CLS Spotorno
33 Terminated A Two Centre Study to Assess the Stability and Long-term Performance of the C-Stem™ AMT in a Total Primary Hip Replacement
Conditions: Rheumatoid Arthritis;   Osteoarthritis;   Post-traumatic Arthritis;   Collagen Disorders;   Avascular Necrosis;   Traumatic Femoral Fractures;   Nonunion of Femoral Fractures;   Congenital Hip Dysplasia;   Slipped Capital Femoral Epiphysis.
Intervention: Device: C-Stem™ AMT Femoral Component (standard and high off-set variants)
34 Terminated A Multi-centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Primary Hip Resurfacing Surgery
Conditions: Rheumatoid Arthritis;   Osteoarthritis;   Post-traumatic Arthritis;   Collagen Disorders;   Avascular Necrosis;   Nonunion of Femoral Fractures;   Congenital Hip Dysplasia;   Slipped Capital Femoral Epiphysis.
Intervention: Device: DePuy ASR Hip System
35 Not yet recruiting Clinical and Radiographic Outcomes of the Corin Tri-Fit Total Hip Replacement
Conditions: Osteoarthritis of Hip;   Congenital Hip Dysplasia;   Avascular Necrosis
Intervention:
36 Active, not recruiting A Multi-centre Study to Assess the Long-term Performance of the Summit™ Hip in Primary Total Hip Replacement
Conditions: Rheumatoid Arthritis;   Osteoarthritis;   Post-traumatic Arthritis;   Collagen Disorders;   Avascular Necrosis;   Traumatic Femoral Fractures;   Nonunion of Femoral Fractures;   Congenital Hip Dysplasia;   Slipped Capital Femoral Epiphysis
Intervention: Device: Summit Tapered Hip System
37 Terminated A Single Centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Primary Hip Resurfacing Surgery
Conditions: Rheumatoid Arthritis;   Osteoarthritis;   Post-traumatic Arthritis;   Collagen Disorders;   Avascular Necrosis;   Nonunion of Femoral Fractures;   Congenital Hip Dysplasia;   Slipped Capital Femoral Epiphysis.
Intervention: Device: DePuy ASR™ Hip System
38 Terminated Post-approval Study of the DURALOC® Option Ceramic-on-Ceramic Hip Prosthesis System
Conditions: Non-inflammatory Joint Disease;   Osteoarthritis;   Avascular Necrosis;   Congenital Hip Dysplasia;   Post-traumatic Arthritis
Interventions: Device: Total hip replacement/arthroplasty;   Device: Hip replacement/arthroplasty
39 Recruiting Transfusion Reaction by Washed Red Blood Cell (RBC)
Conditions: Avascular Necrosis of Hip.;   Degenerative Arthritis, Hip.;   Osteoarthritis, Hip.;   Developmental Dislocation of Hip.;   Dysplastic Hip.
Intervention: Other: Washing of packed RBC by normal saline
40 Terminated A Multi-centre Study to Assess the Long-term Performance of the DePuy PROXIMA™ Hip in Primary Total Hip Replacement
Conditions: Rheumatoid Arthritis;   Osteoarthritis;   Post-traumatic Arthritis;   Avascular Necrosis;   Traumatic Femoral Fractures;   Congenital Hip Dysplasia.
Intervention: Device: DePuy Proxima™ Hip

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Indicates status has not been verified in more than two years