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Ensayo clínico

Assessment of the Verus Frame in Tibial Intramedullary Nailing

NCT: NCT07362121 · RECRUITING

ID NCTNCT07362121
EstadoRECRUITING
Fecha de inicio2026-09-02
SponsorHemitec Finland Oy (INDUSTRY)
First posted
Last updated

Resumen breve

This prospective, single-arm Post-Market Clinical Follow-Up (PMCF) study, utilizing a registry-based control group, will assess the Verus frame's effectiveness in achieving precise tibial rotation and alignment during intramedullary nailing procedure, as well as safety of the device. The results will be compared to AO-approved criteria to ensure comprehensive evaluation of its new benefits, regulatory compliance, and continued clinical use. Tibial intramedullary nailing is the gold standard for tibial fracture fixation, where accurate alignment and rotation are crucial for optimal recovery and long-term outcomes.

Fuente oficial

Ver en ClinicalTrials.gov →

Datos obtenidos de la API de ClinicalTrials.gov. Para conocer el estado más reciente, consulte el registro oficial.

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