Arthritis, Infection of Total Ankle Joint Prosthesis
Conditions
Keywords
Total Ankle Arthroplasty
Brief summary
The primary objective of this study is to collect preoperative, operative and postoperative clinical assessments of patients that qualify for surgical implantation of the INBONE™ Total Ankle Prosthesis.
Detailed description
The FDA approved the limited enrollment registry to provide us with additional clinical data from which to design a pivotal IDE study. FDA has stated that their decision for this was based upon adequate safety information which was submitted to them as part of the original IDE submission. Therefore, the purpose of this limited enrollment registry study is to gather initial data on the device's performance, when used with a Calcaneal Stem.
Interventions
DEVICEINBONE™ Total Ankle Prosthesis with Long Talar Stem
INBONE™ Total Ankle Prosthesis with Long Talar Stem when used with a Calcaneal Stem
Sponsors
Orthopedic Foot and Ankle Center, Ohio
Stryker Trauma and Extremities
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Subject has sufficient soft tissue and muscle strength to support stable, anatomic positioning and motion of arthroplasty components as determined by the investigator 2. Subject must have sufficient skin for wound coverage. 3. Subject demonstrates subtalar joint insufficiency as defined by any of the following: (1)range of motion \<50 percent of the contralateral, non-diseased side (2)pain during physical examination of the subtalar joint (3)fusion AND Subject demonstrates tibio-talar joint insufficiency as defined by any of the following: 1. end stage arthritis as determined by the investigator on plain radiographs 2. pain during physical examination of the tibio-talar joint 3. fusion 4. non-union 5. failed Total Ankle Replacement 4.Subject has Body Mass Index (BMI) \< 40 5.Subject has sufficient calcaneal bone stock as determined by the investigator 6.Subject is able to or capable of providing consent to participate in the clinical investigation and has medical insurance to cover costs associated with their medical care or is willing to assume personal responsibility for costs 7.Subject agrees to comply with this protocol, including participating in required follow-up visits at the investigations site and completing study questionnaires
Exclusion criteria
1. Subject is skeletally immature and under 21 years of age 2. Subject has experienced local or systemic infection within the past twelve months 3. Subject has symptomatic ankle disease or has been treated operatively on the contralateral side 4. Subject has vascular and kidney insufficiencies 5. Subject is suspected to have neuropathy of the foot or ankle 6. Subject has impaired vascular circulation in the affected limb 7. Subject has skin condition that may impair wound healing 8. Subject has known allergy to cobalt, chromium, molybdenum, titanium, aluminum, vanadium, or nickel 9. Subjects on long term medications which may compromise bone stock (e.g. long term steroids, NSAIDS, etc., physicians discretion 10. Subject is unwilling or unable to comply with a rehabilitation program 11. Subject is known to be pregnant, a prisoner, mentally incompetent, and/or alcohol or drug abuser 12. Subject is currently participating in any investigational study not related to this study's preoperative and postoperative care. 13. Subject has rheumatoid arthritis (RA) 14. Subject has been diagnosed with osteoporosis as defined as a DXA t-score \>-2.5.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| to measure the subject's pain, disability and activity level restrictions within the last week. | to measure change from pre-op (baseline) at specified intervals up to 24 months post-op | The FFI, Foot Function Index is a validated self-administered scoring system designed to measure the subject's pain, disability and activity levels within the past week. Possible scores range from 0-100 with a lower score representing less pain, greater function and less restricted ambulation. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Radiographic Evaluation | to measure change from pre-op to post-op at intervals up to 24 months postoperatively. | Standard AP and lateral and oblique x-rays will be obtained at pre-operatively, and at 6 weeks, 3, 6, 12 and 24 months postoperatively. Any standard of care image can be performed 30 days prior to consenting. |
Countries
United States
Outcome results
None listed