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TRIGEN SURESHOT™ Distal Targeting System Study — Sureshot  

Femoral Shaft Fracture Clinical Trial

Official title:
A Prospective, Multi-center, Randomized, Comparison Study of the TRIGEN SURESHOT™ Distal Targeting vs. Standard Targeting Instrumentation

Clinical Trial Summary

The objective of this study is to quantitate the amount of radiation both subjects and surgeons are exposed to during intramedullary nailing of the femur using the TRIGEN SURESHOT Distal Targeting System versus Standard nailing instrumentation.

Clinical Trial Description

The TRIGEN SURESHOT™ Distal Targeting System was designed to be an intraoperative image-guided localization system to aid with drill positioning for screws during intramedullary nailing distal interlocking. It is hypothesized that this system will aid in identification of the distal holes leading to reduced exposure to radiation. The SURESHOT System provides information to the surgeon that is used to place surgical instruments utilizing electromagnetic tracking data obtained intraoperatively. It is indicated for long bone fractures treated with intramedullary nailing in which the use of stereotactic surgery may be appropriate. The hypothesis is that using the TRIGEN SURESHOT™ Distal Targeting System will allow accurate distal locking while effectively decreasing the amount of radiation exposure compared to the standard instrumentation process. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01327508
Study type Interventional
Source Smith & Nephew, Inc.
Contact
Status Terminated
Phase N/A
Start date April 2011
Completion date June 2013
View Details
See also
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