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โ† Trials
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PO vs IV Antibiotics for the Treatment of Infected Nonunion of Fractures After Fixation

RecruitingPhase 3Ages 18 Years - anyAllMajor Extremity Trauma Research Consortium
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In plain words

What the trial is, and whether it could suit you

This is a Phase III clinical randomized control trial to investigate differences between patient with an infected nonunion treated by PO vs. IV antibiotics. The study population will be 250 patients, 18 years or older, being treated for infected nonunion after internal fixation of a fracture with a segmental defect less than one centimeter. Patients will be randomly assigned to either the treatment (group 1) PO antibiotics for 6 weeks or the control group (group 2) IV antibiotics for 6 weeks. The primary hypothesis is that the effectiveness of oral antibiotic therapy is equivalent to traditional intravenous antibiotic therapy for the treatment of infected nonunion after fracture internal fixation, when such therapy is combined with appropriate surgical management. Clinical effectiveness will be measured as the primary outcome as the number of secondary re-admissions related to injury and

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๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: 1. 1\. Bone fracture (proximal to and including the tarsal/metatarsal joint (Lisfranc) or proximal to the carpal joints (includes distal radius fractures), excluding pelvis and spine) that has previously undergone fixation and has not healed and requires fixation to be retained or replaced at least until bone union. Fractures that have not healed and require revision fixation are also eligible. 2. Infection as determined by either 1. FRI criteria 2. CDC criteria (without the timeframe) This includes the possibility of culture negative, but determined to be infection by treating surgeon 3. Systemic antibiotic treatment regimen scheduled for at least 6 weeks Exclusion Criteria: 1. Patients with a high risk of amputation based on the initial managing physician 2. Patients undergoing treatment of any other investigational therapy within the month preceding infection treatment or planned within the 12 months following infection treatment 3. Incarcerated or institutionalized patients 4. Patients who are unable to return for required follow-up visits and/or medical co-morbidities which preclude treatment with a general anesthetic 5. Patients with a prior history of chronic infection at the index site before fracture fixation 6. Patients with pathological fractures from a neoplastic process 7. History of Paget's Disease 8. The patient, or a designated proxy, unwilling to provide consent 9. The patient must be available for follow-up for at least 12 months following infection treatment
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What it tests

  • Standard of Care PO (oral) antibiotics
  • Standard of Care Intravenous (IV) antibiotics
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Where

13 sites
Indiana University
Indianapolis, United States
University of Maryland , MD Department of Orthopaedics
Baltimore, United States
Sinai Hospital Baltimore
Baltimore, United States
Hennepin Health
Minneapolis, United States
Jamaica Hospital Medical Center
Queens, United States
Atrium Health, Carolinas Medical Center
Charlotte, United States
Wake Forest University Baptist Medical Center
Winston-Salem, United States
University of Okalahoma College of Medicine
Oklahoma City, United States

โ€ฆand 5 more on ClinicalTrials.gov.

๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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