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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00764959
Other study ID # PS - 800
Secondary ID
Status Terminated
Phase Phase 4
First received September 30, 2008
Last updated February 8, 2011
Start date October 2007
Est. completion date February 2011

Study information

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

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Device:
Encore Linear™ Hip System
Subjects with degenerative joint disease (DJD), osteoarthritis or rheumatoid arthritis, have received the hip system and are willing to participate in the study.

Locations

Country Name City State
United States Hussamy Orthopedics Vero Beach Florida

Sponsors (1)

Lead Sponsor Collaborator
Encore Medical, L.P.

Country where clinical trial is conducted

United States, 

Outcome

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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