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Assessment of the Verus Frame in Tibial Intramedullary Nailing

Sponsor: Hemitec Finland Oy • ClinicalTrials.gov ID: NCT07362121

Registry updated: 2026-09-18

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Description

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.

Interventions

Verus frame to stabilize tibia (Device)
Verus is used during tibial intramedullary nailing surgery.

Eligibility criteria

Inclusion Criteria: * Tibial fracture to be operated by suprapatellar intramedullary nailing technique * 18-80 years old * Signed informed consent Exclusion Criteria: * Situations where intramedullary fixation is otherwise contraindicated, e.g., active or potential infection, osteoporosis or where a patient's cooperation cannot be guaranteed. * Pregnancy, breastfeeding * Open fractures with severe soft tissue damage * Polytrauma * Previous tibia fracture

Conditions

Tibial Fracture

Locations

Turku University Hospital — Turku, Finland

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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

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