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Active clinical trials for "Hip Dislocation, Congenital"

Results 51-60 of 129

Avenir® Cemented Hip Stem - PMCF

Primary OsteoarthritisPost-Traumatic Osteoarthritis of Hip5 more

The objective of this post-market clinical follow-up study is to confirm the safety and performance of the Avenir® Cemented Hip stem when used in primary total hip arthroplasty.

Active17 enrollment criteria

A Randomised Study to Compare Metal Ion Release and Long-term Performance of the Pinnacle™ Cup With...

OsteoarthritisPost-traumatic Arthritis4 more

The purpose of this study is to monitor the performance and compare the metal ion release of two bearing combinations, ceramic-on-metal and metal-on-metal in the treatment of patients with hip joint disease requiring a total hip replacement. Patients who enter the study will be randomly allocated to one of the bearing combinations and will be evaluated at regular intervals using, patient, clinical and x-ray assessments. Patients will also have blood samples taken at regular intervals to allow the metal ion levels to be determined.

Terminated23 enrollment criteria

Trilogy AB Acetabular Hip System Post Approval Study

OsteoarthritisAvascular Necrosis2 more

This is a post-approval study with prospective enrollment in the United States and a retrospective enrollment outside the United States to obtain functional, quality of life and radiographic data, which will facilitate assessment of the clinical performance of the Zimmer Trilogy AB Acetabular Hip System.

Terminated20 enrollment criteria

Multi-Centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Resurfacing and...

Rheumatoid ArthritisOsteoarthritis6 more

The purpose of this study is to monitor the performance of a large metal-on-metal bearing from the DePuy ASR™ System in the treatment of patients with hip joint disease requiring hip resurfacing surgery or 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. The Study was terminated with effect from 30th November 2011 following the completion of 2 year follow up assessments for those patients remaining in the study. Please note that prior 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/CON155761 and http://www.depuy.com/countries_list.

Terminated23 enrollment criteria

Post-approval Study of the DURALOC® Option Ceramic-on-Ceramic Hip Prosthesis System

Non-inflammatory Joint DiseaseOsteoarthritis3 more

This study is being conducted to gather medium and long-term information regarding the performance and safety of the commercially available DURALOC® Option Ceramic-on-Ceramic Hip Prosthesis System.

Terminated23 enrollment criteria

A Multi-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 December 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.

Terminated14 enrollment criteria

Multi-centre Study to Assess the Long-term Performance of the Deltamotion Cup System in Primary...

Rheumatoid ArthritisOsteoarthritis4 more

The purpose of this study is to monitor the performance of the DeltaMotion cup system 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.

Terminated9 enrollment criteria

A Single Centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Ceramic-on-ceramic...

Rheumatoid ArthritisOsteoarthritis7 more

The purpose of this study is to monitor the performance of the Pinnacle™ Cup with a ceramic-on-ceramic 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.

Terminated13 enrollment criteria

A Randomised Single Centre Study to Compare the Long-term Performance of 4 Designs of the DePuy...

OsteoarthritisPost-traumatic Arthritis6 more

The purpose of this study is to compare the performance of 4 designs of the DePuy Ultima LX hip stem in the treatment of patients with hip joint disease requiring a total hip replacement. Patients who enter the study will be randomly allocated to one of the 4 designs of the DePuy Ultima LX hip stem and will be evaluated at regular intervals following hip surgery using patient, clinical and x-ray assessments.

Terminated2 enrollment criteria

Metal on Metal Versus Metal on Highly Crossed Linked Polyethylene Sytem

OsteoarthritisAvascular Necrosis5 more

This trial will evaluate the 36mm or greater metal head on metal hip system and compare it to the 32mm or 28mm metal head on polyethylene (liner) hip system in patients receiving a primary cementless total hip replacement.

Terminated13 enrollment criteria
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