45 studies found for:    "Developmental dysplasia of hip"
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"Developmental dysplasia of hip" (45 records)
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Rank Status Study
1 Completed Movement Pattern in Patients With Hip Dysplasia
Condition: Hip Dysplasia
Intervention: Procedure: Minimally invasive approach for Periacetabular osteotomy
2 Completed Ultrasound Screening for Developmental Dysplasia of the Hip in Newborns
Condition: Hip Dysplasia
Intervention: Procedure: hip ultrasound
3 Enrolling by invitation Universal Ultrasound-screening for Developmental Dysplasia of the Hip in Newborn
Condition: Developmental Dysplasia of the Hip (DDH)
Intervention: Other: open, prospective cohort-study
4 Enrolling by invitation Stress Analysis of Hip Dysplasia
Condition: Hip Dysplasia
Intervention:
5 Enrolling by invitation Discovering the Gene(s) Causing Developmental Dysplasia of the Hip (DDH)
Condition: Hip Dysplasia
Intervention:
6 Recruiting Functional Capacity After Computer Assisted Periacetabular Osteotomy in Patients With Hip Dysplasia
Condition: Hip Dysplasia
Intervention: Procedure: computer-assisted surgery
7 Completed Treatment for Mild Hip Dysplasia in Newborns
Condition: Developmental Dysplasia of the Hip
Intervention: Device: Abduction treatment
8 Completed Selective Ultrasound Screening for DDH 1991-2006
Condition: Developmental Dysplasia of the Hip
Intervention:
9 Not yet recruiting Evaluation of T1rho Magnetic Resonance Imaging for Diagnosis of Cartilage Lesions in Hips With Developmental Dysplasia
Condition: Developmental Dysplasia of the Hip
Intervention: Other: Gadolinium
10 Unknown  Psychological, Sexually and Social Consequences of Osteoarthritis Treatment With THA or TKA and Joint Preserving Surgery
Conditions: Osteoarthritis;   Depression;   Hip Dysplasia
Intervention:
11 Completed Routine Follow up After Total Hip Arthroplasty Prior Periacetabular Osteotomy
Conditions: Hip Dysplasia;   Osteotomy of Pelvis;   Total Hip Arthroplasty
Intervention: Other: Routine followup
12 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
13 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
14 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)
15 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 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 System
16 Terminated 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
17 Withdrawn A Multi-centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Polyethylene-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 System
18 Terminated Trilogy AB Acetabular Hip System Post Approval Study
Conditions: Osteoarthritis;   Avascular Necrosis;   Congenital Hip Dysplasia;   Traumatic Arthritis
Intervention: Device: Trilogy AB Acetabular Hip Implant System
19 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
20 Terminated 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

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Indicates status has not been verified in more than two years