Tobramycin Injection to Prevent Infection in Open Fractures
Primary Purpose
Wound Infection, Fractures, Open, Surgical Site Infection
Status
Recruiting
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Tobramycin Injection
Sponsored by
About this trial
This is an interventional treatment trial for Wound Infection focused on measuring Local antibiotic, Non-union, Aminoglycoside, Tobramycin, Open extremity fracture, fracture related infection
Eligibility Criteria
Inclusion Criteria:
- Open fracture to arm, leg, or both
- Over the age of 18
Exclusion Criteria:
- Under the age of 18
- Allergy to tobramycin or any other antibiotic in the aminoglycoside family
- Previously treated with a resorbable antibiotic carrier
- Pregnancy
Sites / Locations
- University of KentuckyRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Tobramycin Treatment Group
Standard of Care Treatment Group
Arm Description
Participants in this group receive a local aqueous tobramycin injection (2mg/mL) plus standard of care treatment.
Participants in this group receive standard of care treatment.
Outcomes
Primary Outcome Measures
Rate of infection
Rate of infection one year after open fracture fixation surgery.
Secondary Outcome Measures
Tobramycin effects on non-union
Modified radiographic union score for tibial fracture (mRUST) scores combined with clinical observation of functional weight bearing at 3 months will be assessed. If union status remains unclear, nonunion will be further defined as a need for secondary bone grafting or surgical intervention.
Tobramycin effects on non-union
Modified radiographic union score for tibial fracture (mRUST) scores combined with clinical observation of functional weight bearing at 6 months will be assessed. If union status remains unclear, nonunion will be further defined as a need for secondary bone grafting or surgical intervention.
Tobramycin effects on non-union
Modified radiographic union score for tibial fracture (mRUST) scores combined with clinical observation of functional weight bearing at 12 months will be assessed. If union status remains unclear, nonunion will be further defined as a need for secondary bone grafting or surgical intervention.
Difference in bacterial specification between treatment and standard of care group.
Upon identification of a fracture-related infection within the first 12 months following surgical fixation, sterile intraoperative cultures will be obtained and grown over 21 days to determine bacterial speciation.
Difference in antibiotic resistance between treatment and standard of care group.
Upon identification of a fracture-related infection within the first 12 months following surgical fixation, sterile intraoperative cultures will be obtained and grown over 21 days to determine antimicrobial resistance.
Full Information
NCT ID
NCT04964947
First Posted
July 6, 2021
Last Updated
September 18, 2023
Sponsor
David Landy
Collaborators
United States Department of Defense
1. Study Identification
Unique Protocol Identification Number
NCT04964947
Brief Title
Tobramycin Injection to Prevent Infection in Open Fractures
Official Title
Does Prophylactic Local Tobramycin Injection Lower Open Fracture Infection Rates?
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 10, 2022 (Actual)
Primary Completion Date
September 2025 (Anticipated)
Study Completion Date
September 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
David Landy
Collaborators
United States Department of Defense
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The goal of open extremity fracture (OEF) treatment is to promote fracture healing and restore function while preventing the development of infection. This is achieved through systematic and timely wound debridement and irrigation, fracture stabilization, tetanus prophylaxis, systemic and local antimicrobial therapy, and judicious timing of wound closure based on cleanliness. Early prophylactic systemic antibiotics lower infection rates in open fractures but have limitations of achieving adequate concentration at the hypoperfused wound area. OEF wounds are frequently poor in vasculature secondary to the soft tissue injury, hence adequate concentration of antibiotic cannot permeate to the tissue at risk. If systemic antibiotic concentrations are increased to achieve minimum inhibitory concentration (MIC) for pathogens at the wound, there is heightened concern for systemic drug toxicity. In sharp contrast, locally administered antibiotics achieve high drug concentration directly within the wound cavity with minimal systemic side effects. Local antibiotic therapy has shown to reduce rates of open fracture wound infection. With the serious implications of postoperative infections in OEF, it is imperative that all measures including further use of prophylactic local antibiotics be considered to prevent fracture-related infection (FRI). The overarching hypothesis for this project is that a novel synergistic combination of local aqueous tobramycin plus perioperative weight-based IV cephalosporin antibiotic prophylaxis will reduce the rate of FRI one year after OEF surgery. This in turn will improve OEF patient outcomes, decreasing morbidity and return to the operating room (OR) without any adverse effect on fracture healing. Regardless of the treatment group, bacterial speciation will be determined for patients that do develop FRI to help guide future treatment. The goal is to improve the clinical outcome and recovery of the population that sustains an OEF by decreasing the rate of FRI and fracture nonunions while concurrently educating on bacterial speciation and resistance.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Wound Infection, Fractures, Open, Surgical Site Infection
Keywords
Local antibiotic, Non-union, Aminoglycoside, Tobramycin, Open extremity fracture, fracture related infection
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
300 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Tobramycin Treatment Group
Arm Type
Experimental
Arm Description
Participants in this group receive a local aqueous tobramycin injection (2mg/mL) plus standard of care treatment.
Arm Title
Standard of Care Treatment Group
Arm Type
No Intervention
Arm Description
Participants in this group receive standard of care treatment.
Intervention Type
Drug
Intervention Name(s)
Tobramycin Injection
Intervention Description
80 milligrams of tobramycin diluted in 40 milliliters of normal saline
Primary Outcome Measure Information:
Title
Rate of infection
Description
Rate of infection one year after open fracture fixation surgery.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Tobramycin effects on non-union
Description
Modified radiographic union score for tibial fracture (mRUST) scores combined with clinical observation of functional weight bearing at 3 months will be assessed. If union status remains unclear, nonunion will be further defined as a need for secondary bone grafting or surgical intervention.
Time Frame
3 months after surgery
Title
Tobramycin effects on non-union
Description
Modified radiographic union score for tibial fracture (mRUST) scores combined with clinical observation of functional weight bearing at 6 months will be assessed. If union status remains unclear, nonunion will be further defined as a need for secondary bone grafting or surgical intervention.
Time Frame
6 months after surgery
Title
Tobramycin effects on non-union
Description
Modified radiographic union score for tibial fracture (mRUST) scores combined with clinical observation of functional weight bearing at 12 months will be assessed. If union status remains unclear, nonunion will be further defined as a need for secondary bone grafting or surgical intervention.
Time Frame
12 months after surgery
Title
Difference in bacterial specification between treatment and standard of care group.
Description
Upon identification of a fracture-related infection within the first 12 months following surgical fixation, sterile intraoperative cultures will be obtained and grown over 21 days to determine bacterial speciation.
Time Frame
12 months
Title
Difference in antibiotic resistance between treatment and standard of care group.
Description
Upon identification of a fracture-related infection within the first 12 months following surgical fixation, sterile intraoperative cultures will be obtained and grown over 21 days to determine antimicrobial resistance.
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Open fracture to arm, leg, or both
Over the age of 18
Exclusion Criteria:
Under the age of 18
Allergy to tobramycin or any other antibiotic in the aminoglycoside family
Previously treated with a resorbable antibiotic carrier
Pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Arun Aneja, MD, PhD
Phone
859-323-5533
Email
arun.aneja@uky.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Austin Foster, MD
Phone
859-562-3427
Email
austin.foster@uky.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arun Aneja, MD, PhD
Organizational Affiliation
University of Kentucky
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Kentucky
City
Lexington
State/Province
Kentucky
ZIP/Postal Code
40536
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Arun Aneja, MD, PhD
Phone
859-323-5533
Email
arun.aneja@uky.edu
12. IPD Sharing Statement
Plan to Share IPD
No
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Tobramycin Injection to Prevent Infection in Open Fractures
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