Evaluation of a New Strategy for Protocolized Antibiotic Care for Severe Open Fractures: SEXTANT

Trial ID or NCT#

NCT04678154

Status

recruiting iconRECRUITING

Purpose

The proposed study is a multi-center, prospective randomized controlled trial comparing current standard of care treatment to the SEXTANT treatment protocol in patients with Type III open fractures of the tibia and IIIB fractures of the ankle and hindfoot.

Official Title

Evaluation of a New Strategy for Protocolized Antibiotic Care for Severe Open Fractures: SEXTANT - A Multicenter Randomized Control Trial

Eligibility Criteria

Ages Eligible for Study: 18 Years to 64 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: No
Inclusion Criteria:
  1. 1. Injury meeting at least one of the following criteria:
    1. * Gustilo type III tibia (OTA 41 plateau, OTA 42 shaft and OTA 43 pilon) requiring a second procedure for final debridement and definitive coverage / closure following the index stabilization * Gustilo type IIIB ankle fractures (OTA 44) * Gustilo type IIIB calcaneus fractures (OTA 82) * Gustilo type IIIB talus fractures (OTA 81) * Traumatic "zone-of-injury" trans-tibial amputations requiring DPC, and/or flap coverage2. Ages 18 - 64 years inclusive3. Patients may have risk factors for infection including diabetes, immunosuppression from steroids or other medications, HIV, or other infections.4. Patients may have a traumatic brain injury.5. Patients may have other fractures including spine, upper extremity fractures, contralateral lower extremity injuries, ipsilateral pelvis, hip, femur or foot injuries.6. Patients may be treated initially at an outside institution prior to transfer to the study institution, as long as the definitive wound closure or coverage was not performed prior to entrance into the study.7. Patients with bilateral injuries that meet inclusion criteria may be included, but only the limb rated as "more severe" by the treating surgeon will be enrolled in the study.8. Patients may have co-existing non-tibial or hindfoot infection, with or without antibiotic treatment.9. Patients may be definitively stabilized using any method (nail, plate, ex fix or cast).10. Patients may have a fasciotomy.
Exclusion Criteria:
  1. 1. Patient in current therapy for a wound, implant or fracture site infection related to the study site.2. Patient likely to have difficulty maintaining follow-up, including:
    1. * Diagnosis of a severe psychiatric condition * Intellectually challenged without adequate family support * Resides outside of the hospital's catchment area * Planning to follow-up at another medical center * Being a prisoner * Not having a means of contact (address, cell phone, home phone, e-mail)

Investigator(s)

Michael J. Gardner, MD
Michael J. Gardner, MD
Orthopaedic surgeon, Orthopaedic trauma surgeon
Hatim and Durriya Tyabji Endowed Professor

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Contact

Suna Chung, MPH
4105023357