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Completed
NCT06744907
Safety and Efficacy of Subdermal Betadine During Posterior Spinal Fusion
Conditions: Spinal Fusion
Sex: All
Ages: N/A – 26 Years
Healthy volunteers: No
Phase: PHASE4
Enrollment: 60
Sponsor: Akron Children's Hospital
Location: Akron Children's Hospital Akron Ohio
Summary
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.
Eligibility Criteria
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
Source: ClinicalTrials.gov (NCT06744907). StuddyBuddy aggregates publicly available trial information.