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Clinical Trials in France / NCT06151834
Recruiting Not applicable

Prospective Study of Arthrodesis of Finger Distal Interphalangeal Joints Using the Kerifuse Device

NCT06151834 · tracked via the Priya Life Science France tracker
Sponsor
Clinique Saint François, Nice, France
Phase
Not applicable
Started
2023-12-01
Last updated
2026-07-10

Condition(s) studied

Osteoarthritis FingerOsteoarthritis Thumb

Investigational drug(s) / intervention(s)

KeriFuse implant implantation

KeriFuse implant implantation: The surgery is an arthrodesis of finger or thumb (for patients with finger osteoarthritis) and involves implanting the KeriFuse implant.

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Clinique Saint François Nice France Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06151834 on ClinicalTrials.gov ↗ ← All trials in France