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Distal Locking Using an Electromagnetic Field Guided Computer Based Real Time System for Orthopaedic Trauma Patients (Sure Shot)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01183078
First Posted: August 17, 2010
Last Update Posted: April 13, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
Smith & Nephew, Inc.
Information provided by (Responsible Party):
Wake Forest University Health Sciences
August 11, 2010
August 17, 2010
April 13, 2017
August 2010
September 2013   (Final data collection date for primary outcome measure)
  • Reduced operative time. [ Time Frame: Six months post surgery ]
    The goal is to prospectively assess the "wand" technique as a reliable alternative to standard interlocking screw placement which reduces operative time.
  • Reduced C-arm exposure [ Time Frame: Six months post surgery ]
    The goal is to prospectively assess the "wand" technique as a reliable alternative to standard interlocking screw placement, which reduces C-arm exposure.
  • Reduces inadvertent nail misses. [ Time Frame: Six months post surgery ]
    The goal is to prospectively assess the "wand" technique as a reliable alternative to standard interlocking screw placement, which reduces inadvertent "nail misses."
  • No complications [ Time Frame: Six months post surgery ]
    The goal is to prospectively assess the "wand" technique as a reliable alternative to standard interlocking screw placement. It is expected that there will exist no complications related to the use of this technique.
Reduced operative time. [ Time Frame: Six months post surgery ]
The goal is to prospectively assess the "wand" technique as a reliable alternative to standard interlocking screw placement which reduced operative time, C-arm exposure and inadvertent "nail misses." Additionally, it is expected that there will exist no complications related to the use of this technique.
Complete list of historical versions of study NCT01183078 on ClinicalTrials.gov Archive Site
Not Provided
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Distal Locking Using an Electromagnetic Field Guided Computer Based Real Time System for Orthopaedic Trauma Patients
Distal Locking Using an Electromagnetic Field Guided Computer Based Real Time System for Orthopaedic Trauma Patients
Hypothesis: Utilization of the "wand" method will enhance improvements in drill placement, locking nail placement during tibia and femur fracture repairs, and offer less radiation exposure and less operative time. The purpose of this research study is to compare the efficacy of distal locking of intramedullary nails using a standard free-hand technique with the guided wand technique. Distal locking is the placement of screws through the intramedullary rod to hold it in place and prevent rotation. Currently, the free-hand technique is most often utilized. With this technique, the surgeon uses intraoperative x-rays in order to find the holes in the intramedullary rod to place the screws. The wand technique uses electromagnetic fields rather than x-rays to find these screw holes. The utilization of the wand technique could result in improvements in drill placement and locking nail placement as well as decrease operative time and radiation exposure.

Methods and Measures Patients 18 years of age and older presenting through the emergency room at Wake Forest University Baptist Medical Center with tibial and femoral fractures suitable for operative repair will be prospectively enrolled. Inclusion criteria will include any patient with a tibia fracture or femur fracture requiring intramedullary nailing. Retrograde intramedullary nails will be excluded as will nails which are not interlocked. The goal for enrollment is 24 tibial and 24 femoral fractures. Data including operative time, C-arm time, and "nail misses" will be obtained in the operating room for 24 tibial and 24 femoral nails. Surgeons who perform the procedure will have had experience using the freehand technique and will be trained with the guided wand prior to the experiment. Locking will be performed with the freehand and the wand technique in alternating order for the two interlocking screws. The order of which technique is utilized first will be randomly assigned. All procedures will be timed, and fluoroscopy time, radiation time, and any "nail misses" will be documented. All tibial nails will be locked with 2 mediolateral screws and all femurs with 2 lateral to medial screws.

Patients will receive follow-up for complications for a 6 month period after surgical procedure. Intervals of follow-up will be at 2 weeks, 6 weeks, 3 months and 6 months. Anterior-posterior and lateral images will be performed as are already customary and usual at these time intervals.

Outcome Measure(s) The goal is to prospectively assess the "wand" technique as a reliable alternative to standard interlocking screw placement which reduced operative time, C-arm exposure and inadvertent "nail misses." Additionally, it is expected that there will exist no complications related to the use of this technique.

Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
  • Tibial Fractures
  • Femoral Fractures
  • Procedure: free-hand
    Free-hand technique utilizes x-rays to find screw holes.
  • Procedure: Wand technique
    Wand technique is utilized to find screw holes.
  • Free-hand technique
    Free-hand technique utilized to find screw holes.
    Intervention: Procedure: free-hand
  • Wand technique
    Wand technique is utilized to find screw holes.
    Intervention: Procedure: Wand technique
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
55
September 2013
September 2013   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • 18 years and older with tibial or femoral fracture suitable for operative repair with intramedullary nailing.

Exclusion Criteria:

  • Fractures requiring repair by retrograde intramedullary nails and interlocking nails.
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01183078
IRB00012034
No
Not Provided
Not Provided
Wake Forest University Health Sciences
Wake Forest University Health Sciences
Smith & Nephew, Inc.
Principal Investigator: Riyaz H. Jinnah, MD, FRCS Wake Forest University Health Sciences
Principal Investigator: Eben A. Carroll, MD Wake Forest University Health Sciences
Wake Forest University Health Sciences
January 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP