Prospective Follow-up of the Results of Nail Arthrodesis of the Ankle

N/ANot Yet RecruitingNCT06338566

Direction Centrale du Service de Santé des Armées20 enrolled

Overview

The goal of this prospective, single-center observational study is to describe the functional outcome of the surgical procedure in patient who undergone transplanted centromedullary nailing in the septic setting. Patients will be asked to complete a questionnaire during follow-up consultations.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Ankle Fractures

Interventions

Follow-upOTHER

Follow-up at D45, 3 months and 6 months, with scoring, radiological monitoring and assessment of wound healing

Eligibility

Sex: ALLMin age: 18 YearsMax age: 80 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patient \>18 years * having undergone septic nailing in the operating theatre * with social security coverage Exclusion Criteria: * Patient with 6-month follow-up not possible (medical wandering, transient patient), * Patient who has benefited from another means of osteosynthesis * Patients whose long-term return to weight-bearing will not be possible for reasons other than ankle arthrodesis surgery. * Persons able to give consent but unable to read or write French * Opposes participation in the study * Patients whose cognitive capacity does not allow them to answer questionnaires

Outcomes

Primary Outcomes

bony outcome of transcalcaneal nailing

percentage of patients with aseptic consolidation at 6 months post-op

Time frame: up to 6 months

Secondary Outcomes

functional result of the procedure

percentage of patients able to walk again at 6 months post-op

Time frame: up to 6 months

Data from ClinicalTrials.gov

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