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Traumatic Arthritis of Hip clinical trials

View clinical trials related to Traumatic Arthritis of Hip.

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NCT ID: NCT05186168 Active, not recruiting - Osteoarthritis, Hip Clinical Trials

Corin MiniHip and Trinity Cup Clinical Surveillance Study

Start date: March 15, 2011
Phase:
Study type: Observational

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.

NCT ID: NCT00551967 Active, not recruiting - Clinical trials for Osteoarthritis of Hip

Evaluation of the Wear of Vitamin E Treated Polyethylene Components in Primary THA Using RSA

Start date: October 2007
Phase: N/A
Study type: Interventional

The specific aim of this proposed study is to conduct a prospective RSA clinical study at Massachusetts General Hospital involving 50 patients receiving primary total hip replacements. All patients will receive the vitamin E treated polyethylene acetabular inserts. Short-term femoral head penetration and long-term steady state wear of the polyethylene will be measured using both RSA and Martell analysis techniques. Stability of the acetabular and femoral components will be measured in all patients using RSA analysis. The stability of the cemented femoral stems will be compared to the stability of the cementless femoral components as well as to historic data in the literature. In addition, all patients will complete a self-administered questionnaire to assess the clinical outcome of the surgery and patient satisfaction.

NCT ID: NCT00545285 Active, not recruiting - Clinical trials for Osteoarthritis of Hip

Long-Term Multi-center Evaluation of E-Poly and Regenerex

Start date: November 2007
Phase: N/A
Study type: Interventional

There are two distinct aims of this study: 1. This prospective study is designed to document the long-term (10-year) radiographic and clinical outcomes of a new type of highly cross-linked polyethylene liner which contains vitamin E as an anti-oxidant, (E-Poly), in a group of primary total hip arthroplasty subjects. The clinical outcome of E-Poly will be compared to a group of subjects receiving Arcom XL polyethylene. 2. This study is also designed to document the long-term (10-year) radiographic and clinical outcomes of a new cementless acetabular component having a titanium porous surface (Regenerex). The clinical outcome of this new FDA cleared device will be compared a group of subjects receiving an acetabular component having a plasma sprayed surface.