Status:
RECRUITING
3D Multisegment Foot Model Used for the Clinical Outcome After Ankle and Hindfoot Reconstruction
Lead Sponsor:
Universitaire Ziekenhuizen KU Leuven
Conditions:
Ankle and Hindfoot Alterations
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
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 th...
Detailed Description
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 th...
Eligibility Criteria
Inclusion
- Being routinely scheduled for a reconstructive surgical procedure for the following indications or involving the following type of procedure:
- Any reconstructive procedure for Pes Planus, Pes Plano-valgus, or Posterior Tibial Tendon Dysfunction
- Tibio-talar arthrodesis or prosthesis
- Sub-talar -and/or (partial) Chopart - and/or Triple arthrodesis
- Pantalar arthrodesis with or without inclusion of the Chopart joint
Exclusion
- Age under 18
- Need of tools (eg walker or crutches) to walk less than 100m
- Inability to walk less than 100 m anyway
- Differences in leg length exceeding 3 cm (measured clinically)
- Extreme in-or outtoeing
- Subjects with BMI \> 27.5 require very careful further consideration whether or not the obesity prevents the accurate palpation of anatomical landmarks necessary prior to marker placement. This will be judged on an individual basis.
Key Trial Info
Start Date :
March 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2025
Estimated Enrollment :
300 Patients enrolled
Trial Details
Trial ID
NCT04822558
Start Date
March 1 2013
End Date
December 1 2025
Last Update
November 12 2024
Active Locations (1)
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1
UZ Leuven
Leuven, Vlaams-Brabant, Belgium, 3000