Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04822558

3D Multisegment Foot Model Used for the Clinical Outcome After Ankle and Hindfoot Reconstruction

Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2026-03-13

300

Participants Needed

1

Research Sites

717 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Most symptomatic pathologies of the ankle and hindfoot are determined by biomechanical alterations of this anatomical region. Surgical treatment of these pathologies is therefore aimed at improving the inferior biomechanical condition, and it can be expected that an improvement of the biomechanical parameters grossly parallels the targeted clinical improvement. 3D Multisegment Foot Models have been developed and validated to determine the clinical outcome. Such a validated 3D Multisegment Foot Model is now standard available in the gaitlab of UZ Leuven making it possible to study a huge amount of biomechanical parameters within the foot \& ankle region itself.

CONDITIONS

Official Title

3D Multisegment Foot Model Used for the Clinical Outcome After Ankle and Hindfoot Reconstruction

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Scheduled for reconstructive surgery for Pes Planus, Pes Plano-valgus, or Posterior Tibial Tendon Dysfunction
  • Scheduled for Tibio-talar arthrodesis or prosthesis
  • Scheduled for Sub-talar, partial Chopart, and/or Triple arthrodesis
  • Scheduled for Pantalar arthrodesis with or without Chopart joint involvement
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Need tools like a walker or crutches to walk less than 100 meters
  • Unable to walk at least 100 meters
  • Leg length difference greater than 3 centimeters
  • Extreme inward or outward foot rotation (in-toeing or out-toeing)
  • Body mass index (BMI) over 27.5 unless individual assessment confirms accurate marker placement is possible

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UZ Leuven

Leuven, Vlaams-Brabant, Belgium, 3000

Actively Recruiting

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Research Team

G

Giovanni Matricali

CONTACT

K

Kevin Deschamps

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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