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Functional and Radiological Outcome after Distal Tibiofibular Arthrodesis for Chronic Instability

Functional and Radiological Outcome after Distal Tibiofibular Arthrodesis for Chronic Instability - Distal tibiofibular arthrodesis

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON35599
Enrollment
11
Registered
2011-11-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Synostosis / distal tibiofibular arthrodesis

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Adult patients: >18 years All patients who were treated with a distal tibiofibular arthrodesis (creation of a synostosis) for chronic syndesmotic instability (more than 6 months after initial trauma).

Exclusion criteria

Exclusion criteria: Patients younger than 18 years at time of follow up.

Design outcomes

Primary

MeasureTime frame
Functional assessment - AOFAS ankle scores, American Orthopaedic Foot & Ankle Society (AOFAS) ankle-hindfoot clinical rating scale - Foot Ankle Ability Measure (FAAM) - Foot and Ankle Outcome Score (FAOS) Radiological assessment - arthritis scores (van Dijk et al./ Kellgren and Moore / etc.)—

Secondary

MeasureTime frame
Perceived disability as quantified by the following scoring system: - SF-36 - Range of motion - Patient overall satisfaction with the outcome of the procedure on a NRS - Complications - Re-operations - Adverse events—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)