Condition: Cutaneous Leishmaniasis · Sponsor: Hayder Adnan Fawzi
Aim of the study to evaluate the effectiveness of intralesional levofloxacin 0.5% solution as a local injection in treating cutaneous leishmaniasis. In an open-label single-arm clinical trial, all patients were given intralesional levofloxacin injections; the patients had cutaneous leishmaniasis lesions. Each lesion was considered a case in the final analysis. Each lesion will be followed up for 90 days (censor endpoint) or until the lesions are cured. Intralesional levofloxacin (5 mg/ml, 100 ml, Tavanic®, Sanofi, France) will be injected into each lesion based on its size (5 mg/cm2). The infiltration of intralesional dose will be given once weekly for up to 6 weeks. Treatment will be stopped in patients cured before 6 weeks of treatment. A fine insulin needle will be used to infiltrate the lesion.
This description comes directly from the study's public registry record.
Hayder Adnan Fawzi, PhD · 07800106177 · haider-pharm@almustafauniversity.edu.iq
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| Mustansiriyah University | Baghdad, Iraq | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06797544