RecruitingNCT05484089

CapFlex PIP Implant RSA

Migration of the CapFlex-PIP Implant System for Proximal Interphalangeal Joint Arthroplasty: a 10 Year Follow up RSA Study


Sponsor

Reinier Haga Orthopedisch Centrum

Enrollment

36 participants

Start Date

Oct 25, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

Rationale: Patients with osteoarthrtis (OA) of the proximal interphalangeal (PIP) joint are commonly treated with joint arthroplasty. The CapFlex PIP implant is a modular surface replacing implant, which has good short-term functional results with a relatively low complication rate. To reduce implant failure and to increase long-term survival, it is important to expand knowledge about fixation and loosening patterns. By using model-based roentgen stereogrammaetric analysis (mRSA), the migration pattern of the implant over time can be calculated. Objective: The primary objective is to assess the fixation and migration patterns of the CapFlex PIP implant system (produced and developed by several companies of KLS Martin Group) in vivo, using mRSA, over 10 years. Secondary objectives are to analyse survival, clinical scores and radiographic aspects of the CapFlex PIP implant system. Study design: A prospective cohort study with 10 years follow-up, in which 36 patients will be enrolled. Patients will be evaluated preoperatively, at 6 weeks, 6 months, 1 year, 2 years 5 years and 10 years. Study population: Patients 18 years or older who require a proximal interphalangeal joint arthroplasty as a result of osteoarthritis of a proximal interphalangeal joint. Main study parameters/endpoints: The main study parameters are the migration of the CapFlex PIP implant system of the distal as well as the proximal component (presented in x-, y- and z-direction). Secondary study parameters are the survival of the CapFlex PIP implant system, clinical scores and radiographic aspects. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Patients participating in the study will have the same risks when not participating in the study. Patients are asked to spend time to fill in the questionnaires and to have 3 extra visits to the hospital, next to the standard visits. Patients will have more follow up visits and will be followed using RSA analysis, which has as advantage that possible complications might be noticed earlier compared to normal follow up.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study uses a special X-ray technique (RSA — radiostereometric analysis) to measure the movement and stability of the CapFlex PIP finger joint implant over time. It helps researchers understand how well this artificial joint performs in patients with arthritis or finger fractures. You may be eligible if: - You are over 18 years old - You need a PIP (proximal interphalangeal) finger joint replacement due to painful osteoarthritis or a severe intra-articular fracture - You speak and write Dutch - You are willing to participate and can give written consent You may NOT be eligible if: - You have inflammatory arthritis with significant bone loss - You have insufficient bone quality for a stable implant - You have a known allergy to the implant materials - This would be a revision (repeat) surgery - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICECapFlex PIP implant

Patients receive the CapFlex PIP implant based on regular care. During surgery tantalum markers are placed in the bone surrounding the implant.


Locations(1)

Reinier Haga Orthopedisch Centrum

Zoetermeer, South Holland, Netherlands

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NCT05484089


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