Prospective Study of Arthrodesis of Finger Distal Interphalangeal Joints Using the Kerifuse Device
Recruiting · NCT06151834 · Interventional (participants receive a specific treatment) · Lead sponsor: Clinique Saint François, Nice, France
View the official record on ClinicalTrials.gov →Interventions studied
What this trial is about
Arthrodesis of a distal interphalangeal joint of the finger (DIP) is mainly performed for a degenerated and painful joint. Various stabilization methods have been used to provide compression at the arthrodesis site such as pins, steel wires, compression screws, headless compression screws, bioresorbable implants and intramedullary staples. Although with complications such as implant fractures or dorsal cortical erosion, intramedullary arthrodesis staples provide reliable pain relief and a consistent fusion rate while inevitably scarring the finger pulp or nail dystrophy. The aim of this study is to evaluate the bone fusion time during an arthrodesis performed with the Kerifuse shape memory implant.
Who can take part
Inclusion criteria
- Eligible patients with osteoarthritis of finger for an interphalangeal arthrodesis with KeriFuse implant
Exclusion criteria
- Pregnant or breastfeeding patient
- Patient with an intellectual disability and who therefore cannot follow the surgeon's instructions
- Patients with contraindications to surgery
- Patients with acute or chronic, local or systemic infections
- Patients with sensitivities or allergies to device components (Nickel, Titanium)
Where it is running
1 location listed.
- Clinique Saint François - Nice, France