Post-PMA Approval Study: 10 Year Follow-Up IDE Subjects

Completed

Conditions studied: Osteoarthritis, Avascular Necrosis, Rheumatoid Arthritis

In brief

primary endpoint of this Study is maintenance of "at least good clinical status" for a period of 10 years following initial implantation among Cormet procedures enrolled inthe pre-market IDE.

Key facts

Study ID

NCT00721994

Run by

Corin

People needed

231

Starts

2008-05-01

Expected to finish

2017-08-01

Last updated by the study team

2018-11-21

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• subjects enrolled in the Cormet IDE study at the 5 identified clinical sites
• Individuals who agree to participate in the study by signing the informed patient consent form

You may not qualify if…

• none

Where it is running

• Space Coast Orthopaedics Ctr. — Merritt Island, Florida, United States
• Kennedy White Orthopedics — Sarasota, Florida, United States
• Southern Illinois University School of Medicine — Springfield, Illinois, United States
• Good Samaritan Hospital — Baltimore, Maryland, United States
• Cleveland Center for Joint Reconstruction — Cleveland, Ohio, United States

Full record on ClinicalTrials.gov

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