Rheumatoid Arthritis Clinical Trial
Official title:
Post-Market Study of the Linear™ Hip System
Verified date | February 2011 |
Source | Encore Medical, L.P. |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Observational |
The purpose of this study is to evaluate the use and efficacy of the Encore Linear™ Hip System in a group of 200 patients for whom data has already been collected.
Status | Terminated |
Enrollment | 200 |
Est. completion date | February 2011 |
Est. primary completion date | February 2011 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Have hip joint disease related to one or more of the following - osteoarthritis - rheumatoid arthritis - femoral fracture - correction of a functional deformity - avascular necrosis of the natural femoral head - Skeletal maturity - Patient is likely to be available for evaluation for the duration of the study - Able and willing to sign the informed consent and follow study procedures - Patient is not pregnant - No infection present - No known materials sensitivity - Patient is over 18 years of age Exclusion Criteria: - Skeletal immaturity - Infection or sepsis - Insufficient bone quality that may affect the stability of the implant - Muscular, neurologic or vascular deficiencies which compromise the affected extremity - Alcoholism or other addictions - Prisoners - High levels of physical activity - Patient is pregnant - Loss of ligamentous structures - Materials sensitivity - Patient is under 18 years of age |
Observational Model: Cohort, Time Perspective: Retrospective
Country | Name | City | State |
---|---|---|---|
United States | Hussamy Orthopedics | Vero Beach | Florida |
Lead Sponsor | Collaborator |
---|---|
Encore Medical, L.P. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The use and efficacy of the Encore Linear™ Hip System | 2 year | No |
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