Long Term Follow-up of Integra® Cadence™ Total Ankle System in Primary Ankle Joint Replacement
| 适应症 | Degenerative Arthritis, Rheumatoid Arthritis, Traumatic Arthritis |
|---|---|
| 分期 | 不适用 |
| 申办方 | Smith & Nephew, Inc. |
| 状态 | 提前终止 |
| 受试者人数 | 65 人 |
| 干预（药物） | Implantation of Integra Cadence Total Ankle System |
| 开始日期 | 2017年9月18日 |
| 完成日期 | 2023年9月6日 |
| 结果公布日 | 2026年6月22日 |
摘要
This study will evaluate the long term performance and safety data for the Cadence™ Total Ankle System (CTAS) when used for primary arthroplasty in patients with primary arthritis (e.g. degenerative disease), secondary arthritis (e.g. post-traumatic, avascular necrosis, if minimally 2/3 of the talus is preserved), and systemic arthritis of the ankle (e.g. rheumatoid arthritis, hemochromatosis)
Implant Survivorship at 2 Years
| Integra® Cadence™ Total Ankle System | 100 percentage of participants |
|---|
在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文
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- CD40L Antagonism in Rheumatoid Arthritis (RA) — National Institute of Allergy and Infectious Diseases (NIAID)
- A Study of Baricitinib in Participants With Rheumatoid Arthritis — Eli Lilly and Company
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