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Clinical Trial Summary

Ankel fractures is a common fracture. Most patients experience that the regain normal range of motions and limited pain within the first 6 months following ankel fracture, but not all. The aim of the study is to determine if any prognostic factors is associated with a worse outcome.


Clinical Trial Description

Aim of study: To identify prognostic factors associated with a worse outcome following ankle fractures. Method: All operated or non-operated ankle fractures in a period of one year from three different hospitals will be included. The following data will be recorded: Civil registration number, age, rupture of the syndesmosis, use of alcohol, smoking, diabetes, characteristics of the ankle fracture (AO classification), type of treatment and complications. Study participants will at time of diagnosis and 6, 12, 52 and 104 weeks following the injury received a questionaire with Manchester foot and ankle questionnaire (MOXFQ), Self-reported foot and ankle questionnaire (SEFAS), Olerud Molander Ankle Score (OMAS) and Forgotten Joint Score (FJS). Which of the questionaire that should be used in the study will be determined when the questionaires have been compared in a different study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03741556
Study type Observational [Patient Registry]
Source Sygehus Lillebaelt
Contact
Status Completed
Phase
Start date November 7, 2018
Completion date October 1, 2022

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