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Distal Targeter vs Free-hand

Primary Purpose

Femur Fracture, Tibial Fractures, Nonunion of Fracture

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Distal targeting jig
Free-hand/perfect circles technique
Sponsored by
Cedars-Sinai Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Femur Fracture focused on measuring femur fracture, tibia fracture, operative time, screw placement, jig

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: 18 years old and above Undergoing intramedullary fixation of femur or tibia shaft for acute fracture or nonunion Exclusion Criteria: Prior ipsilateral tibial or femoral nail Patients who cannot have interlocking screws placed Pregnant women

Sites / Locations

  • Cedars Sinai Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Free-hand/perfect circles

Distal targeting jig

Arm Description

Patients in this group will have interlocking screw placement using a free-hand, perfect circles technique.

Patients in this group will have interlocking screw placement using a proximally placed distal targeting jig

Outcomes

Primary Outcome Measures

Patient Radiation exposure
Number of fluoroscopic images taken intraoperatively for screw placement and cumulative radiation exposure (in grays)
Total screw placement time
time taken to place interlocking screws
Measurement of Screw Placement Angle
Correct screw placement is at a right (90-degree) angle from the intramedullary nail, through the interlocking screw hole

Secondary Outcome Measures

Learning curve
learning curve between distal targeter and freehand techniques stratified by level of training
Training methods
Correlation of sawbones-based practice and clinical practice for interlocking screw placement with regards to time taken for screw placement and accuracy of screw placement (deviation from right angle relative to intramedullary device)

Full Information

First Posted
October 31, 2022
Last Updated
August 7, 2023
Sponsor
Cedars-Sinai Medical Center
Collaborators
Stryker Nordic
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1. Study Identification

Unique Protocol Identification Number
NCT05613257
Brief Title
Distal Targeter vs Free-hand
Official Title
A Randomized Controlled Trial Comparing Free-Hand Versus Distal Targeting Jig-Based for Distal Interlock Screw Placement
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 31, 2022 (Actual)
Primary Completion Date
October 1, 2023 (Anticipated)
Study Completion Date
October 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cedars-Sinai Medical Center
Collaborators
Stryker Nordic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is a randomized controlled trial comparing the use of two different surgical techniques--free-hand versus distal targeting jig-based for distal interlock screw--placement and their effects on total operative time and intraoperative radiation exposure.
Detailed Description
Interlocking screw placement in intramedullary nailing of femoral and tibial shaft fractures improves rotational and length stability. However, free-hand perfect circle techniques can be technically challenging and may take up to an hour with increased radiation exposure to the surgeon and patient. Newer technologies aimed at reducing fluoroscope use such as electromagnetically-based aiming devices may increase the operative time. Proximally-based jigs have been shown to reduce fluoroscopy time in cadavers, however, have not been studied clinically. This study is a prospective, randomized controlled trial comparing a modern proximally-based distal targeting device and free-hand techniques for placement of interlocking screws in lower extremity nailing.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Femur Fracture, Tibial Fractures, Nonunion of Fracture, Nonunion of Fracture of Tibia, Nonunion of Fracture of Femur (Diagnosis), Tibia Fracture
Keywords
femur fracture, tibia fracture, operative time, screw placement, jig

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients will be randomly assigned to cohorts based on the operative technique used to treat their respective fractures.
Masking
Participant
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Free-hand/perfect circles
Arm Type
Active Comparator
Arm Description
Patients in this group will have interlocking screw placement using a free-hand, perfect circles technique.
Arm Title
Distal targeting jig
Arm Type
Experimental
Arm Description
Patients in this group will have interlocking screw placement using a proximally placed distal targeting jig
Intervention Type
Device
Intervention Name(s)
Distal targeting jig
Intervention Description
Patients in this arm will have an assistive targeting device used for interlocking screw placement. The targeting device is attached to the nail proximally or distally (for antegrade or retrograde nailing, respectively) to guide screw placement through the other end of the intramedullary device.
Intervention Type
Procedure
Intervention Name(s)
Free-hand/perfect circles technique
Intervention Description
Patients in this arm will have no assistive targeting device use and the surgeon will use a free-hand technique for the placement of interlocking screws. With this technique, fluoroscopic images are taken such that the interlocking holes of the intramedullary device are "perfect circles" and indicate that a screw introduced in the same plane that the fluoroscopic image was taken would seat perpendicularly to the intramedullary device. This is the most commonly employed technique for interlocking screw placement through intramedullary devices.
Primary Outcome Measure Information:
Title
Patient Radiation exposure
Description
Number of fluoroscopic images taken intraoperatively for screw placement and cumulative radiation exposure (in grays)
Time Frame
During surgery: The first fluoroscopy shot for distal interlocking screw placement to final fluoroscopy shot confirming the final screw's placement
Title
Total screw placement time
Description
time taken to place interlocking screws
Time Frame
During surgery: the first fluoroscopy shot to localize the jig or obtain a perfect circle (start) to the last shot to confirm complete seating of the screw (end time)
Title
Measurement of Screw Placement Angle
Description
Correct screw placement is at a right (90-degree) angle from the intramedullary nail, through the interlocking screw hole
Time Frame
Intraoperatively (at end of surgery)
Secondary Outcome Measure Information:
Title
Learning curve
Description
learning curve between distal targeter and freehand techniques stratified by level of training
Time Frame
Through study completion (6 month study period)
Title
Training methods
Description
Correlation of sawbones-based practice and clinical practice for interlocking screw placement with regards to time taken for screw placement and accuracy of screw placement (deviation from right angle relative to intramedullary device)
Time Frame
Through study completion (6 month study period)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years old and above Undergoing intramedullary fixation of femur or tibia shaft for acute fracture or nonunion Exclusion Criteria: Prior ipsilateral tibial or femoral nail Patients who cannot have interlocking screws placed Pregnant women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Laura Sarmiento, CCRP
Phone
310-423-4295
Email
laura.sarmiento@cshs.org
First Name & Middle Initial & Last Name or Official Title & Degree
Joel Arnold
Phone
310-423-4614
Email
joel.arnold@cshs.org
Facility Information:
Facility Name
Cedars Sinai Medical Center
City
Los Angeles
State/Province
California
ZIP/Postal Code
90048
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Laura Sarmiento, CCRP
Phone
310-423-4295
Email
laura.sarmiento@cshs.org
First Name & Middle Initial & Last Name & Degree
Kevin Huang, MS
Phone
310-423-2844
Email
kevin.huang3@cshs.org
First Name & Middle Initial & Last Name & Degree
Carol A Lin, MD
First Name & Middle Initial & Last Name & Degree
Charles N Moon, MD
First Name & Middle Initial & Last Name & Degree
John M Garlich, MD
First Name & Middle Initial & Last Name & Degree
Geoffrey S Marecek, MD
First Name & Middle Initial & Last Name & Degree
Milton T Little, MD
First Name & Middle Initial & Last Name & Degree
Mark S Vrahas, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
24714403
Citation
Maqungo S, Horn A, Bernstein B, Keel M, Roche S. Distal interlocking screw placement in the femur: free-hand versus electromagnetic assisted technique (sureshot). J Orthop Trauma. 2014 Dec;28(12):e281-3. doi: 10.1097/BOT.0000000000000125.
Results Reference
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PubMed Identifier
9781891
Citation
Miclau T, Holmes W, Martin RE, Krettek C, Schandelmaier P. Plate osteosynthesis of the distal femur: surgical techniques and results. J South Orthop Assoc. 1998 Fall;7(3):161-70.
Results Reference
background
PubMed Identifier
16310192
Citation
Whatling GM, Nokes LD. Literature review of current techniques for the insertion of distal screws into intramedullary locking nails. Injury. 2006 Feb;37(2):109-19. doi: 10.1016/j.injury.2005.09.009. Epub 2005 Nov 28.
Results Reference
background
PubMed Identifier
32259266
Citation
Program of Randomized Trials to Evaluate Pre-operative Antiseptic Skin Solutions in Orthopaedic Trauma (PREP-IT) Investigators; Slobogean GP, Sprague S, Wells J, Bhandari M, Rojas A, Garibaldi A, Wood A, Howe A, Harris AD, Petrisor BA, Mullins DC, Pogorzelski D, Marvel D, Heels-Ansdell D, Mossuto F, Grissom F, Del Fabbro G, Guyatt GH, Della Rocca GJ, Demyanovich HK, Gitajn IL, Palmer J, D'Alleyrand JC, Friedrich J, Rivera J, Hebden J, Rudnicki J, Fowler J, Jeray KJ, Thabane L, Marchand L, O'Hara LM, Joshi MG, Talbot M, Camara M, Szasz OP, O'Hara NN, McKay P, Devereaux PJ, O'Toole RV, Zura R, Morshed S, Dodds S, Li S, Tanner SL, Scott T, Nguyen U. Effectiveness of Iodophor vs Chlorhexidine Solutions for Surgical Site Infections and Unplanned Reoperations for Patients Who Underwent Fracture Repair: The PREP-IT Master Protocol. JAMA Netw Open. 2020 Apr 1;3(4):e202215. doi: 10.1001/jamanetworkopen.2020.2215. Erratum In: JAMA Netw Open. 2020 Sep 1;3(9):e2021571. JAMA Netw Open. 2021 Jun 1;4(6):e2117240.
Results Reference
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Distal Targeter vs Free-hand

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