34 studies found for:    "Developmental dysplasia of hip"
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Rank Status Study
1 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
2 Recruiting Efficacy and Satisfaction Comparing Two Braces in the Treatment of Developmental Dysplasia of the Hip (DDH) in Infants
Conditions: Hip Dislocation, Congenital;   Congenital Deformity of Hip Joint
Interventions: Other: Pavlik Brace;   Other: Plastizote Brace
3 Completed Selective Ultrasound Screening for DDH 1991-2006
Condition: Developmental Dysplasia of the Hip
Intervention:
4 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
5 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
6 Withdrawn A Multi-centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Polyethylene-on-metal Bearing in Primary Total Hip Replacement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
7 Recruiting AMIStem Primary Hip System Prospective Post-marketing Multi-centre Surveillance Study
Conditions: Osteoarthritis;   Arthritis;   Avascular Necrosis;   Fracture of the Femoral Neck or Head;   Congenital Hip Dysplasia
Intervention: Device: AMIStem Hip System
8 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
9 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)
10 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
11 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
12 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
13 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
14 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
15 Completed EBIS: The Eindhoven Breech Intervention Study
Conditions: Breech Presentation;   External Cephalic Version;   Thyroid Hormones;   Stress, Psychological;   Congenital Hip Dysplasia
Intervention:
16 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
17 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
18 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
19 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
20 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)

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Indicates status has not been verified in more than two years