A Prospective International Hip Dysplasia Registry with Follow-up to Skeletal Maturity: An Analysis of Risk Factors Screening Practices and Treatment Outcomes

Brief description of study

The purpose of this study is to develop a general prospective registry that includes all elements of the DDH spectrum, from mild dysplasia of a reduced hip, to an irreducible dislocation. This international data registry for developmental dysplasia of the hip (DDH) will allow for a better understanding of treatments for children with hip dysplasia and to determine which treatments may be the most beneficial for children with hip dysplasia.

Clinical Study Identifier: s17-00096
Principal Investigator: Pablo G. Castaneda.

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