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NOT YET RECRUITING
NCT07362121
NA

Assessment of the Verus Frame in Tibial Intramedullary Nailing

Sponsor: Hemitec Finland Oy

View on ClinicalTrials.gov

Summary

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.

Official title: Assessment of the Verus Frame as a Support for the Leg in Orthopaedic Surgery (Intramedullary Nailing) of Tibial Fracture in Adults. A Prospective, Single-arm, Interventional Post-market Clinical Investigation With AO Foundation Approved Acceptance Criteria and a Retrospective Registry Control Group.

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

25

Start Date

2026-05-01

Completion Date

2027-05

Last Updated

2026-01-23

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Verus frame to stabilize tibia

Verus is used during tibial intramedullary nailing surgery.

Locations (1)

Turku University Hospital

Turku, Finland