Proximal Phalanx Fractures Registry

Brief description of study

The purpose of this study is to prospectively collect data and observe clinical outcomes following the treatment of proximal phalanx fractures with SOC modalities, including but not limited to closed reduction percutaneous pinning (CRPP), open reduction internal fixation (ORIF), and treatment with headless compression screws (HCS). Patients will be recruited and observed prospectively throughout the duration of their treatment. The approximate sample size will be 200 patients who present at NYU and related sites who have had a proximal phalanx fracture. Demographic data will be collected at initial visit and participants will be then be followed and observed longitudinally to determine the outcome of standard of care treatment options.

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