New Method for Distal Interlocking of Cannulated Intramedullary Nails

Status Terminated

Clinical Trial Summary

We intend to include10 patients in this study and trial. Prior to treatment they will sign an informed consent form, stating that they are acquainted with the surgical procedure and study, and that they consent to participate in the study.

Five patients will undergo regular operation with Universal tibial reamed nail (AO-Synthes) using the fluoroscopy device: OEC 9800 (GENERAL ELECTRIC). five patients will undergo the same operation using the new navigation system:"The Guiding star" method.

The allocation will be random.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Diagnostic

Related Conditions & MeSH terms

Fracture

Clinical Trial Details

NCT number	NCT00648479
Study type	Interventional
Source	Hadassah Medical Organization
Contact
Status	Terminated
Phase	Phase 1/Phase 2

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