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Ligamentous injury after supination trauma of the ankle and foot: Is a ligamentous avulsion fracture an indicator of extensive ligamentous injury? An MRI-based study.

Ligamentous injury after supination trauma of the ankle and foot: Is a ligamentous avulsion fracture an indicator of extensive ligamentous injury? An MRI-based study. - SToF

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON57665
Enrollment
45
Registered
2024-12-09
Start date
2026-03-06
Completion date
Unknown
Last updated
2026-03-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

avulsion fracture foot

Interventions

n.a.

Sponsors

Isala
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: - Aged between 18 and 50 years at the time of the study entry - Presenting to ED within 48 hours after supination trauma of the ankle, with swelling and/or tenderness on the dorsolateral side of the foot. - Radiographically confirmed cuboid/navicular avulsion fracture, or suspected ligamentous injury based on trauma mechanism and clinical examination. - Competent to understand the study and participate in follow ups consisting of completing Dutch questionnaires.

Exclusion criteria

Exclusion criteria: - A significant fracture identified on standard radiographs that, according to  the current guidelines, requires urgent (surgical) treatment.  - A history of previous injuries or conditions affecting the same foot (e.g.  prior fractures, osteoarthritis, repetitive ankle strains). - A history of systemic chronic joint-related diseases (e.g. rheumatoid  arthritis) or active gout.  - Any neurological or musculoskeletal disorders affecting gait or balance (e.g.  peripheral neuropathy, multiple sclerosis). - Current use of medications that may impair healing (e.g. corticosteroids,  immunosuppresants). - Active infection or open wounds in the affected foot or ankle.  - Prior surgical intervention on the affected foot or ankle. - Patients with contraindications for MRI (e.g. metallic implants, pacemaker). - Participation in another clinical trial that could interfere with the  outcomes of this study.

Design outcomes

Primary

MeasureTime frame
The main study parameter in this study is the identification of additional ligament injuries using MRI.

Secondary

MeasureTime frame
Secondary study parameters include the extent of these additional ligament injuries, assessed in terms of quantity and severity, as well as the presence of other soft tissue injuries and factors influencing the functional outcomes of patients.

Countries

Netherlands

Contacts

Public ContactI Christofides

Isala

onderzoek.orthopedie@isala.nl08 624 8117

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Mar 20, 2026