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Rochester, Minn.
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A Comparison of Infection Rates Between Two Surgical Sites
Location:
Rochester, Minn.
Trial status:
Open for Enrollment
Why is this study being done?
The intent of this proposed prospective observational cohort study is to determine if there is a difference in the incidence of corneal toxicity and/or ototoxicity in study subjects undergoing Mohs micrographic surgery (MMS) on the face if a povidone-iodine preparation is used pre-operatively as compared to a chlorhexidine-alcohol preparation. It has recently been found that the use of a chlorhexidine-alcohol preparation is superior to the use of a povidone-iodine preparation in preventing post-operative surgical-site infections (SSI) in patients undergoing clean-contaminated surgery. However, the use of chlorhexidine on the face has previously been associated with corneal toxicity and ototoxicity. This study will help to further define previously reported risks of corneal toxicity and ototoxicity associated with the use of a chlorhexidine solution on the face.
NCT ID:
NCT01263262
IRB Number:
10-004643
Who can I contact for additional information about this study?
Rochester: Jerry Brewer, MD