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Active clinical trials for "Hip Dislocation, Congenital"

Results 41-50 of 129

PMCF Study on the Safety and Performance of the Zimmer® Maxera™ Acetabular System in Total Hip Arthroplasty...

Rheumatoid Arthritis With Adequate Bone QualityInflammatory Arthritis5 more

This study is a multicenter, prospective, non-controlled post market clinical follow-up study. The objectives of this study are to confirm the safety and performance of the commercially available Zimmer® Maxera™ Acetabular System in Total Hip Arthroplasty.

Active43 enrollment criteria

The Medacta International AMIStem-P Post-Marketing Surveillance Study

ArthrosisTraumatic Arthritis3 more

This is a Post-Market Surveillance study of AMIStem-P femoral stem prosthesis

Active11 enrollment criteria

Post Market Clinical Follow-up of EUROSTEM Femoral Stem

Hip OsteoarthritisHip Arthropathy4 more

EUROSSTEM is intended for use in primary and revision total hip replacement surgery. Hip replacement is intended to provide increased patient mobility and reduce pain by replacing the damages hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. As part of post market vigilance, EUROS will collect data on EUROSTEM performances and safety

Active6 enrollment criteria

Post Market Clinical Follow-up of EUROSCUP Fixe Acetabular Cup

Hip ArthropathyHip Osteoarthritis4 more

EUROSCUP Fixe is intended for use in primary and revision total hip replacement surgery. Hip replacement is intended to provide increased patient mobility and reduce pain by replacing the damages hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. As part of post market vigilance, EUROS will collect data on EUROSCUP Fixe performances and safety

Active6 enrollment criteria

A Single Centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Primary Hip...

Rheumatoid ArthritisOsteoarthritis6 more

The purpose of this study is to monitor the performance and determine the metal ion release of the DePuy ASR™ System in the treatment of patients with hip joint disease requiring hip resurfacing surgery. Patients who enter the study will be evaluated at regular intervals following hip surgery using patient, clinical and x-ray assessments. A subset of patients will also have blood samples taken at regular intervals to allow the metal ion levels to be determined and undergo scans to allow the bone mineral density of the bone surrounding the implant to be monitored. DePuy decided to close this Study in 4Q 2009. The Study was terminated with effect from November 2010 to allow for the completion of the 5 year follow up assessments. Please note that subsequent to this decision DePuy voluntarily recalled the ASR products on 24 August 2010. Additional information regarding this voluntary recall and the follow-up of patients affected by the recall can be found at the following links http://www.mhra.gov.uk/Publications/Safetywarnings/MedicalDeviceAlerts/CON079157 and http://www.depuy.com/countries_list.

Terminated17 enrollment criteria

A Two Centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Metal-on-Metal...

Rheumatoid ArthritisOsteoarthritis7 more

The purpose of this study is to monitor the performance and determine the metal ion release of the Pinnacle™ Cup with a metal-on-metal bearing combination in the treatment of patients with hip joint disease requiring a total hip replacement. Patients who enter the study will be evaluated at regular intervals following hip surgery using patient, clinical and x-ray assessments. A subset of patients will also have blood samples taken at regular intervals to allow the metal ion levels to be determined.

Terminated16 enrollment criteria

AVANTAGE® RELOAD Double Mobility Acetabular Cup -Clinical Study

Primary OsteoarthritisPost-Traumatic Arthritis6 more

This is a Post Marketing Clinical Follow Up study (PMCF) on the AVANTAGE RELOAD dual mobility system cup.

Active24 enrollment criteria

Prospective Study for the Evaluation of the Cementless Anatomic Femoral Stem Minimax -Launay

Primary OsteoarthritisSecondary Osteoarthritis6 more

This is a post-marketing surveillance on MiniMAX Stem

Active15 enrollment criteria

Corin MiniHip and Trinity Cup Clinical Surveillance Study

Total Hip ArthroplastyOsteoarthritis5 more

The aim of the study is to provide long term follow up data on the performance and safety of the Corin MiniHip and Trinity acetabular cup over a 10-year period.

Active23 enrollment criteria

Sequelae of Developmental Dysplasia of the Hip

Developmental Dysplasia of the HipHip Dysplasia

The aim of this study is to assess long term effects of developmental dysplasia of the hip (DDH) to overall health and quality of life later in life. We compare hip radiographs, hip symptoms, clinical examination, head asymmetry, dental examination and intraoral scans of 170 children and young adults treated for DDH in their childhood with age and sex matched controls.

Active4 enrollment criteria
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