Effectiveness and Safety of the Silicone Joint Implant KeriFlex® and of Its Associated Instruments in the Treatment of MCP and PIP Arthritis: Post Market Clinical Follow up
Status: Recruiting
Location: See all (3) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY
The general objective of this study is to assess the performance and safety of the KeriFlex® silicone joint implant and its associated instruments, used in accordance with the labeling and instructions in force. The performance and safety of the KeriFlex® joint implant will be established in the short and long term with regard to the life cycle of the implant.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Adult patients (age ≥ 18 years)
• Patients who are going to undergo arthroplasty of the metacarpophalangeal or proximal interphalangeal joint using a KeriFlex® implant in accordance with the instructions for use and the labelling in force.
• Patients with rheumatoid arthritis, osteoarthritis or post-traumatic osteoarthritis
Locations
Other Locations
France
CHU Jean Minjoz
RECRUITING
Besançon
Clinic Lille Sud
RECRUITING
Lesquin
Institut aquitain de la main et du membre supérieur
RECRUITING
Pessac
Contact Information
Primary
CAUX
clinic@kerimedical.com
058 255 01 30
Time Frame
Start Date: 2023-11-14
Estimated Completion Date: 2035-01
Participants
Target number of participants: 86
Related Therapeutic Areas
Sponsors
Leads: Keri Medical SA