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Lange termijn resultaten na een enkelartrodese

Follow-up of patients with an ankle arthrodesis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON23848
Enrollment
30
Registered
2018-10-11
Start date
2018-11-01
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

ankle arthrodesis, arthritis, artrodese, arthrodese, enkel, artrose

Interventions

This is an observational study in which patients that have had an ankle arthrodesis will be asked to visit the Erasmus MC for a follow-up visit. During this follow-up visit a bilateral CAT-scan of the

Sponsors

Erasmus Medical Center, Department of Orthopaedics
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Received a primary ankle arthrodesis at the department of Orthopaedics of the Erasmus MC between 1-1-2004 until 31-12-2016 - A pre-operative CAT-scan of the operated ankle is available

Exclusion criteria

Exclusion criteria: - Received a double or triple arthrodesis - Arthrodesis with an intramedullary nail or external fixator - Amputation of the ankle after the arthrodesis - Patient deceased

Design outcomes

Primary

MeasureTime frame
Degree of arthritis in de adjacent joints (subtalar joint and talonavicular joint) in patients that have had an ankle arthrodesis

Secondary

MeasureTime frame
(1) the amount of increase of arthritis in the adjacent joints compared to before surgery, (2) the degree of arthritis in the contralateral ankle, (3) the correlation between degree of arthritis and patient reported outcomes

Contacts

Public ContactA. Willems
a.willems@erasmusmc.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)