RecruitingNot ApplicableNCT07592325

Clinical Evaluation of the Access Socket Flexible Socket for Transtibial Prosthesis


Sponsor

Union de Gestion des Etablissements des Caisses d'Assurance Maladie - Nord Est

Enrollment

25 participants

Start Date

Apr 27, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Transtibial amputation significantly impacts patient autonomy and quality of life, primarily due to the limitations of conventional rigid sockets, which restrict comfort and joint range of motion. The Access Socket (AS) is an innovative prosthetic socket combining a rigid carbon-fiber structure in key load-bearing areas with flexible urethane-resin (ProtheFLEX®) zones in regions typically rigid in conventional sockets. This hybrid design aims to improve comfort and pressure distribution while preserving the mechanical properties required for ambulation. The AS has already demonstrated benefits in transfemoral amputees and is now reimbursed in France for that population. A preliminary uncontrolled study in 12 transtibial amputees suggested significant improvements in perceived function, comfort, satisfaction, and mobility. This multicenter, randomized, open-label, two-arm crossover study aims to compare the (AS) with the standard rigid socket (RS) in 25 adults with transtibial amputation. Participants will wear each socket for approximately 4 weeks (after a 1-2 week adaptation period) in a randomized order. The primary outcome is the Patient Specific Functional Scale (PSFS). Secondary outcomes include comfort (SCS), satisfaction (OPUS), psychosocial adjustment (TAPES-R), mobility (PLUS-M), prosthesis utility (PEQ-U), and the proportion of patients electing to keep the AS at study completion.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Access Socket (AS) and a medical device called Rigid Socket (RS) for people with lower limb amputation below knee and transtibial amputation. The study is currently recruiting participants at 5 locations.

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

DEVICEAccess Socket (AS)

Hybrid prosthetic socket combining a rigid carbon-fiber structure in load-bearing areas (lateral, postero-inferior, inferior) with flexible urethane-resin (ProtheFLEX®) zones in regions typically rigid in conventional sockets. Manufactured from the same plaster mold as the rigid socket to ensure identical internal geometry.

DEVICERigid Socket (RS)

Conventional definitive carbon-fiber rigid socket, currently the only socket type reimbursed in France for transtibial amputation (LPPR-listed). Standard of care comparator.


Locations(5)

Hôpital National d'Instruction des Armées (HNIA) Percy

Clamart, France

Hôpital Filieris de Freyming-Merlebach

Freyming-Merlebach, France

CHU Grenoble Alpes - Hôpital Sud

Grenoble, France

Institut Régional de Médecine Physique et de Réadaptation (IRR) - Filière Locomoteur

Nancy, France

Insititution Nationale des Invalides

Paris, France

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NCT07592325


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