Characterizing the biomechanics and morphology of posterior tibial tendon dysfunction
Biomechanical and Morphological Characterization of the Foot in Patients With Posterior Tibial Tendon Dysfunction.
This study is trying to better understand the changes in the foot caused by posterior tibial tendon dysfunction to help doctors make better treatment choices for patients dealing with this painful condition.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | Universitaire Ziekenhuizen KU Leuven Academic / other |
| Locations | 1 site (Leuven, Vlaams-Brabant) |
| Trial ID | NCT06260813 on ClinicalTrials.gov |
What this trial studies
This study focuses on posterior tibial tendon dysfunction (PTTD), a progressive condition that leads to severe foot deformities and pain. It aims to enhance clinical decision-making by integrating biomechanical and morphological characteristics into the existing classification system for PTTD. The study will utilize various imaging techniques, including radiography, ultrasound, MRI, and CT scans, along with gait analysis to assess the condition across different stages. By understanding these characteristics, the study seeks to improve treatment strategies for affected patients.
Who should consider this trial
Good fit: Ideal candidates include adults aged 18-675 with varying stages of posterior tibial tendon dysfunction.
Not a fit: Patients who are younger than 18, unable to walk without aids, or have significant leg length discrepancies may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to more effective and personalized treatment options for patients with posterior tibial tendon dysfunction.
How similar studies have performed: While there is existing research on PTTD, this study's focus on integrating biomechanical and morphological assessments is a novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion criteria: * Patient groups: * Posterior tibial tendon dysfunction (all clinical stages) * Age 18-675 year * ICF obtained * Control group: * No pain complaints * No pes plano valgus, PTTD or pes cavo varus or other foot and ankle pathology * Age 18-75 year * ICF obtained Exclusion criteria patient and control groups: * Being younger than 18 years * Inability to walk without mobility aids * Inability to walk \< 100 meter * Difference in leg length \> 3cm * Subjects with BMI\>30 kg/m², due to less accurate gait analysis by absence of anatomical landmarks * Subjects unable to perform a gait analysis * Any medical condition possibly affecting normal gait. * Pregnancy: at the start or during the study
Where this trial is running
Leuven, Vlaams-Brabant
- UZ Leuven — Leuven, Vlaams-Brabant, Belgium (Recruiting)
Study contacts
- Principal investigator: Sander Wuite — Universitaire Ziekenhuizen KU Leuven
- Study coordinator: Sander Wuite
- Email: sander.wuite@uzleuven.be
- Phone: +32 16 33 83 29
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.