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Gentamicin Open Tibia Study (GO-Tibia)

Primary Purpose

Fracture Open Tibia

Status
Recruiting
Phase
Phase 4
Locations
Tanzania
Study Type
Interventional
Intervention
Gentamicin
normal Saline
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Fracture Open Tibia

Eligibility Criteria

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

Inclusion Criteria:

  • Age>18 years old
  • Open tibial shaft fracture meeting the following criteria:

    1. Orthopaed Trauma Association (OTA) Type 42
    2. Primarily closable wound
    3. Gustilo-Anderson (GA) Type I, II, or IIIA

Exclusion Criteria:

  • Time from injury to presentation > 48 hours
  • Time from injury to surgery > 7 days
  • Aminoglycoside allergy
  • GA IIIB or IIIC open fractures
  • Bilateral open tibial fractures
  • Severe brain (GCS<12) or spinal cord injury
  • Severe vascular injury
  • Severe burns (>10% Total Body Surface Area (TBSA) or >5% TBSA with full thickness or circumferential injury)
  • Pathologic fracture
  • History of active limb infection, ipsilaterally
  • Unlikely to complete follow-up

Sites / Locations

  • Muhimbili Orthopaedic InstituteRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Gentamicin

Saline

Arm Description

The intervention consists of 80mg of liquid gentamicin diluted in 5 mL normal saline (16mg/mL). The solution is injected by inserting a 22-gauge needle down to bone through an anteromedial approach at the level of the fracture site such that the injected solution fills the wound cavity. A total of 5mL of study solution will be administered.

The control consists of 5 mL normal saline injected immediately after wound closure at the open fracture site. The solution is injected by inserting a 22-gauge needle down to bone through an anteromedial approach at the level of the fracture site such that the injected solution fills the wound cavity. A total of 5mL of study solution will be administered.

Outcomes

Primary Outcome Measures

Occurrence of fracture-related infection (FRI)
Fracture-related infection is a consensus definition of infection after fracture treatment. It is diagnosed by an orthopaedic surgeon based on any of the following four diagnostic criteria: (1) fistula, sinus or wound breakdown; (2) purulent drainage from the wound or presence of pus during surgery; (3) phenotypically indistinguishable pathogens identified by culture from at least two separate deep tissue/implant specimens; or (4) presence of microorganisms in deep tissue taken during an operative intervention, as seen on histopathological examination. FRI diagnosis is likely to peak between 6 weeks and 6 months after surgery and has a non-normal time-to-event distribution, with incident cases rarely presenting later than 12 months after surgery. All events will be confirmed by an independent adjudication committee comprised of three masked, non-treating orthopaedic trauma surgeons.

Secondary Outcome Measures

Occurrence of nonunion
Binary outcome based on the following criteria: Any unplanned reoperation for promotion of bone healing; OR Modified Radiographic Union Scale for Tibia Fractures (mRUST) ≤10 at 12 months follow-up AND either: Function IndeX for Trauma (FIX-IT) score ≤11 at 12 month follow-up, OR recommendation by treating surgeon for nonunion repair surgery
Occurrence of unplanned fracture-related reoperation
Occurrence of unplanned fracture-related reoperation, a binary variable, for infection, wound healing, or fracture union, excluding removal of implants for prominence/irritation. This may include but is not limited to: Irrigation and debridement of surgical incisions or open fracture wounds due to infections or wound healing problems; Revision wound closure for dehiscence; Soft tissue coverage procedure for infected or necrotic wound; Fracture delayed union or nonunion surgery (such as bone grafting or implant exchange); Reoperation for hardware or prosthesis failure due to infection or bone-healing problems; Amputation for infection, wound or fracture healing problem.
Health-related quality-of-life (HRQOL) as measured by EQ-5D-3L (Swahili version)
The EQ-5D is a survey instrument that assesses multiple domains of quality-of-life, including mobility, self-care, usual activities, pain/discomfort and anxiety/depression.
Fracture healing by modified Radiographic Union Scale for Tibial fractures (mRUST score)
The mRUST score is based on evaluation plain radiographs of the fracture site. Each cortex is scored from 1-4 based on the degree of healing and summed resulting in an ordinal scale ranging from 4 to 16, with higher score indicating greater fracture healing.
Clinical fracture healing by Function IndeX for Trauma (FIX-IT)
The FIX-IT score is an ordinal scale from 0-12 that encompasses two domains: ability to weight-bear and pain at fracture site, each scored from 0-6. Higher score indicates more clinical healing.
Occurence of FRI Suggestive Criteria
Suggestive criteria are signs/symptoms of infection that do not meet criteria for definitive fracture-related infection (FRI). These include clinical signs (wound redness, fever) and radiographic signs (sequestrum), elevated serum inflammatory markers, and new onset or increased non-purulent wound drainage.

Full Information

First Posted
November 30, 2021
Last Updated
September 2, 2022
Sponsor
University of California, San Francisco
Collaborators
Muhimbili Orthopaedic Institute, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), Orthopedic Research and Education Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT05157126
Brief Title
Gentamicin Open Tibia Study
Acronym
GO-Tibia
Official Title
A Masked, Randomized Controlled Trial Evaluating Locally-applied Gentamicin Versus Saline in Open Tibia Fractures
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2022 (Actual)
Primary Completion Date
April 2028 (Anticipated)
Study Completion Date
April 2029 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
Muhimbili Orthopaedic Institute, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), Orthopedic Research and Education Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Local application of antibiotics directly to the traumatic wound is a promising treatment for the prevention of infection after open tibia fractures, which are a significant source of disease burden globally, particularly in low-income countries. This study aims to measure the effect of locally applied gentamicin on risk of infection for open tibial fractures in Tanzania. If proven effective, local gentamicin would be a highly cost-effective strategy to reduce complications and disability from open tibial fractures that could impact care in both high- and low-income countries.
Detailed Description
Tibial shaft (shinbone) fractures are the most common major fracture of the lower leg and are frequently associated with a break in the skin known as an open fracture. Because the bone is exposed by the open wound, open tibial fractures are often complicated by infection and failure of bone healing, which can lead to long-lasting disability and in some cases amputation. Intravenous antibiotics administered early after injury are a well-established measure to prevent fracture-related infection (FRI), but their effectiveness is limited by poor blood flow at the fracture site and inability to achieve high local concentrations with systemic administration. Gentamicin applied locally within the open fracture wound is a promising adjunctive measure to reduce the risk of FRI after these injuries, but there are no high-quality clinical trials evaluating its use. This will be the first randomized trial evaluating locally administered gentamicin to reduce infection in a fracture population. If efficacious, local gentamicin is likely to be a highly cost-effective preventive strategy for FRI and may ultimately be cost saving. Although these findings will originate from a low-income country, results may be generalizable to populations in both high and low-income countries and could therefore significantly reduce the global burden of open fractures.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fracture Open Tibia

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Single-center individually-randomized placebo-controlled superiority trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Data collectors (research coordinators) and data analysts will also be masked
Allocation
Randomized
Enrollment
890 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Gentamicin
Arm Type
Experimental
Arm Description
The intervention consists of 80mg of liquid gentamicin diluted in 5 mL normal saline (16mg/mL). The solution is injected by inserting a 22-gauge needle down to bone through an anteromedial approach at the level of the fracture site such that the injected solution fills the wound cavity. A total of 5mL of study solution will be administered.
Arm Title
Saline
Arm Type
Placebo Comparator
Arm Description
The control consists of 5 mL normal saline injected immediately after wound closure at the open fracture site. The solution is injected by inserting a 22-gauge needle down to bone through an anteromedial approach at the level of the fracture site such that the injected solution fills the wound cavity. A total of 5mL of study solution will be administered.
Intervention Type
Drug
Intervention Name(s)
Gentamicin
Intervention Description
Liquid gentamicin administered at the open fracture site
Intervention Type
Drug
Intervention Name(s)
normal Saline
Intervention Description
Normal saline administered at the open fracture site
Primary Outcome Measure Information:
Title
Occurrence of fracture-related infection (FRI)
Description
Fracture-related infection is a consensus definition of infection after fracture treatment. It is diagnosed by an orthopaedic surgeon based on any of the following four diagnostic criteria: (1) fistula, sinus or wound breakdown; (2) purulent drainage from the wound or presence of pus during surgery; (3) phenotypically indistinguishable pathogens identified by culture from at least two separate deep tissue/implant specimens; or (4) presence of microorganisms in deep tissue taken during an operative intervention, as seen on histopathological examination. FRI diagnosis is likely to peak between 6 weeks and 6 months after surgery and has a non-normal time-to-event distribution, with incident cases rarely presenting later than 12 months after surgery. All events will be confirmed by an independent adjudication committee comprised of three masked, non-treating orthopaedic trauma surgeons.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Occurrence of nonunion
Description
Binary outcome based on the following criteria: Any unplanned reoperation for promotion of bone healing; OR Modified Radiographic Union Scale for Tibia Fractures (mRUST) ≤10 at 12 months follow-up AND either: Function IndeX for Trauma (FIX-IT) score ≤11 at 12 month follow-up, OR recommendation by treating surgeon for nonunion repair surgery
Time Frame
12 months
Title
Occurrence of unplanned fracture-related reoperation
Description
Occurrence of unplanned fracture-related reoperation, a binary variable, for infection, wound healing, or fracture union, excluding removal of implants for prominence/irritation. This may include but is not limited to: Irrigation and debridement of surgical incisions or open fracture wounds due to infections or wound healing problems; Revision wound closure for dehiscence; Soft tissue coverage procedure for infected or necrotic wound; Fracture delayed union or nonunion surgery (such as bone grafting or implant exchange); Reoperation for hardware or prosthesis failure due to infection or bone-healing problems; Amputation for infection, wound or fracture healing problem.
Time Frame
12 months
Title
Health-related quality-of-life (HRQOL) as measured by EQ-5D-3L (Swahili version)
Description
The EQ-5D is a survey instrument that assesses multiple domains of quality-of-life, including mobility, self-care, usual activities, pain/discomfort and anxiety/depression.
Time Frame
12 months
Title
Fracture healing by modified Radiographic Union Scale for Tibial fractures (mRUST score)
Description
The mRUST score is based on evaluation plain radiographs of the fracture site. Each cortex is scored from 1-4 based on the degree of healing and summed resulting in an ordinal scale ranging from 4 to 16, with higher score indicating greater fracture healing.
Time Frame
12 months
Title
Clinical fracture healing by Function IndeX for Trauma (FIX-IT)
Description
The FIX-IT score is an ordinal scale from 0-12 that encompasses two domains: ability to weight-bear and pain at fracture site, each scored from 0-6. Higher score indicates more clinical healing.
Time Frame
12 months
Title
Occurence of FRI Suggestive Criteria
Description
Suggestive criteria are signs/symptoms of infection that do not meet criteria for definitive fracture-related infection (FRI). These include clinical signs (wound redness, fever) and radiographic signs (sequestrum), elevated serum inflammatory markers, and new onset or increased non-purulent wound drainage.
Time Frame
12 months
Other Pre-specified Outcome Measures:
Title
Adverse events
Description
All serious and non-serious adverse events will be reported as counts for each treatment group
Time Frame
12 months
Title
Fold-change in creatinine level
Description
Creatinine is a laboratory value used to assess kidney function. Creatinine levels will be measured preoperatively and 2-days postoperatively for all study participants.
Time Frame
2 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age>18 years old Open tibial shaft fracture meeting the following criteria: Orthopaed Trauma Association (OTA) Type 42 Primarily closable wound Gustilo-Anderson (GA) Type I, II, or IIIA Exclusion Criteria: Time from injury to presentation > 48 hours Time from injury to surgery > 7 days Aminoglycoside allergy GA IIIB or IIIC open fractures Bilateral open tibial fractures Severe brain (GCS<12) or spinal cord injury Severe vascular injury Severe burns (>10% Total Body Surface Area (TBSA) or >5% TBSA with full thickness or circumferential injury) Pathologic fracture History of active limb infection, ipsilaterally Unlikely to complete follow-up
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
David W Shearer, MD, MPH
Phone
628-206-8812
Email
david.shearer@ucsf.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Tigist Belaye, MPA
Phone
628-206-8812
Email
tigist.belaye@ucsf.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David W Shearer, MD, MPH
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Billy T Haonga, MD
Organizational Affiliation
Muhimbili Orthopaedic Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Muhimbili Orthopaedic Institute
City
Dar es Salaam
Country
Tanzania
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Billy T Haonga, MD
Phone
255-022-2151298
First Name & Middle Initial & Last Name & Degree
Billy T Haonga, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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Gentamicin Open Tibia Study

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