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Study identifier: NCT07592325 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Clinical Evaluation of the Access Socket Flexible Socket for Transtibial Prosthesis

Condition: Transtibial Amputation · Lower Limb Amputation Below Knee  ·  Sponsor: Union de Gestion des Etablissements des Caisses d'Assurance Maladie - Nord Est

PhaseNA
Planned participants25
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Isabelle Loiret, MD  ·  +33383529950  ·  isabelle.loiretpro@gmail.com

Jonathan Pierret, PhD  ·  jonathan.pierret@ugecam.assurance-maladie.fr

Always discuss trial participation with your own doctor first.

Locations (5)

Hôpital National d'Instruction des Armées (HNIA) PercyClamart, FranceRecruiting
Hôpital Filieris de Freyming-MerlebachFreyming-Merlebach, FranceRecruiting
CHU Grenoble Alpes - Hôpital SudGrenoble, FranceRecruiting
Institut Régional de Médecine Physique et de Réadaptation (IRR) - Filière LocomoteurNancy, FranceRecruiting
Insititution Nationale des InvalidesParis, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07592325