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Efficacy of Oral Antibiotic Therapy Compared to Intravenous Antibiotic Therapy for Osteomyelitis (CRO-OSTEO)

Loyola University logo

Loyola University

Status and phase

Terminated
Phase 2

Conditions

Osteomyelitis

Treatments

Drug: Intravenous Antibacterial Agent
Drug: Oral Antibacterial Agent

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The Infectious Diseases Society of America (IDSA) 2012 guidelines for the diagnosis and treatment of diabetic foot infections state that for the treatment of diabetic foot osteomyelitis "No data support the superiority of any specific antibiotic agent or treatment strategy, route, or duration of therapy." Traditionally, osteomyelitis has been treated with a long course of intravenous antibiotics, generally six weeks. Oral antibiotics with high bioavailability and adequate bone penetration have been shown in published studies to be effective for the treatment of osteomyelitis.

The investigators propose to conduct a prospective, single-center, randomized, open trial at Loyola University Medical Center (LUMC) comparing the efficacy of oral antibiotic therapy to intravenous (IV) antibiotic therapy for the treatment of diabetic foot osteomyelitis. The investigators hypothesize that oral antibiotic therapy is equivalent to IV antibiotic therapy. Bone/tissue cultures are obtained for all patients for clinical purposes and are sent to pathology for histologic examination and to the clinical microbiology laboratory for culture and susceptibility. Patients will receive six weeks of IV or oral antibiotic therapy depending upon their randomization group. Primary outcomes at six months clinical follow-up will include: (i) no evidence of bone infection and (ii) resolution of ulcer.

Full description

Currently, available literature is not adequate to determine the best agent, route, or duration of antibiotic therapy for the treatment of chronic osteomyelitis. The standard of therapy has been to treat patients with a parenteral antibiotic for four to six weeks. In a recent literature review by Spellberg et al. it was concluded that oral and parenteral antibiotic therapy have similar cure rates for the treatment of chronic osteomyelitis. Oral antibiotic therapy is associated with a lower risk to the patient due to avoiding the need of a central IV line. Additionally, oral therapy costs less than a course of IV antibiotics. Oral antibiotics with high bioavailability and good bone penetration include, fluoroquinolones, linezolid, trimethoprim/sulfamethoxazole (2 tabs bid), clindamycin and metronidazole. These antibiotics have been shown in recent studies to obtain levels in the bone that exceed the minimum inhibitory concentration (MIC) levels of the targeted organisms. According to the IDSA 2012 guidelines for the treatment of diabetic foot infections, the diagnosis of osteomyelitis can be made via plain radiographs or MRI imaging (more sensitive). A bone scan can be considered if an MRI cannot be done. The preferred method of diagnosis is by bone culture and histology. The guidelines also recommend surgical debridement to healthy tissue for diabetic foot infections followed by antibiotic therapy.

The Purpose of this study is to compare the efficacy of oral antibiotic therapy with intravenous antibiotic therapy for the treatment of diabetic foot osteomyelitis following surgical debridement. They hypothesis is that oral antibiotic therapy is equivalent to intravenous antibiotic therapy for the treatment of diabetic foot osteomyelitis.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years of age and older
  • Diagnosis of Diabetes Mellitus (per past medical history documented in the patient medical record)
  • Foot osteomyelitis (distal to ankle)
  • Surgical debridement (in operating room)

Exclusion criteria

  • Absolute neutrophil count (ANC) < 500
  • Pregnant or lactating patients
  • Patients with organisms resistant to oral therapy
  • Internal hardware
  • Definitive amputations (BKA)
  • Limb ischemia [absent pedal pulses or ankle-brachial index (ABI) < 0.5]

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 3 patient groups

Midfoot
Active Comparator group
Description:
Individuals with an infection on the midfoot are randomized to an intravenous antibacterial agent or an oral antibacterial agent.
Treatment:
Drug: Oral Antibacterial Agent
Drug: Intravenous Antibacterial Agent
Hindfoot
Active Comparator group
Description:
Individuals with an infection on the hindfoot are randomized to an intravenous antibacterial agent or an oral antibacterial agent.
Treatment:
Drug: Oral Antibacterial Agent
Drug: Intravenous Antibacterial Agent
Toe
Active Comparator group
Description:
Individuals with an infection on the toe are randomized to an intravenous antibacterial agent or an oral antibacterial agent.
Treatment:
Drug: Oral Antibacterial Agent
Drug: Intravenous Antibacterial Agent

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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