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Safety and Efficacy of Subdermal Betadine During Posterior Spinal Fusion

RecruitingPhase 4Ages any - 26 YearsAllAkron Children's Hospital
NCT06744907 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

Bacterial in the subdermal layer of the skin, such as in hair follicles and sweat glands, may contaminate surgical wounds. The goal of this study is to learn about povidone-iodine and its ability to prevent infections specifically in patients with scoliosis receiving a spinal fusion.

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📋 Eligibility rules (as published)
Inclusion Criteria * Males and females * Undergoing primary posterior spinal fusion of the thoracic and/or lumbar spine * English Speaking Exclusion Criteria * Patients who have undergone prior spinal surgery * Undergoing procedures other than primary posterior spinal fusion of the thoracic and/or lumbar spine (cervical fusion, anterior surgery, growth-friendly instrumentation) * Any contraindication to povidone-iodine, including pregnancy, allergy, or prior treatment with radioiodine
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What it tests

  • 10% Povidone-Iodine Arm
  • Saline Arm
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Where

1 site
Akron Children's Hospital
Akron, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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