Condition: Cutaneous Leishmaniasis · Sponsor: Al-Mustafa University College
The Aim of the trial to evaluate the effectiveness of intralesional ciprofloxacin 0.2% solution as a local injection in treating cutaneous leishmaniasis and compare its effect with intralesional sodium stibogluconate (SSG) 10% intravenous solution in cutaneous leishmaniasis as a local injection. In a randomized parallel groups clinical trial, patients were divided into two groups based on therapeutic regimen: 1) intralesional sodium stibogluconate weekly injection and 2) intralesional ciprofloxacin injection. 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.
This description comes directly from the study's public registry record.
Hayder Adnan Fawzi, PhD · 009647800106177 · haider-pharm@almustafauniversity.edu.iq
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| Mustansiriyah University | Baghdad, Iraq | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06798402