Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 3:01 PM
Ignite Modification Date:
2025-12-24 @ 3:01 PM
NCT ID:
NCT01790659
Eligibility Criteria:
Inclusion Criteria:
* Male or female at least 2 years-of-age
* Subject or legal guardian able to give written informed consent or assent, as appropriate
* Diagnosis of CL in at least one lesion by at least one of the following methods: 1) positive culture for promastigotes or 2) microscopic identification of amastigotes in stained lesion tissue
* At least one ulcerative lesion ≥ 1 cm and ≤ 5 cm that has a diagnosis of CL
* Willing to forego other forms of treatments for CL including other investigational treatments during the study
* In the opinion of the investigator, subject (or their legal guardian), subject is capable of understanding and complying with the protocol
* If female and of child-bearing potential, must have a negative serum pregnancy test during screening and agree to use an acceptable method of birth control during the treatment phase and for 1 week after treatment is completed
Exclusion Criteria:
* Lesion due to leishmania that involves the nasal or oral mucosa or any signs of mucosal disease that might be due to Leishmania
* Only a single lesion on the ear with erosive cartilage
* Signs and symptoms of disseminated disease in the opinion of the investigator
* More than 10 lesions
* Female who is breast-feeding
* Significant organ abnormality, chronic disease such as diabetes, severe hearing loss, evidence of renal or hepatic dysfunction, or creatinine, aspartate aminotransferase (AST), or alanine aminotransferase (ALT) greater than 15% above the upper limit of normal (ULN) as defined by the clinical laboratory defined normal ranges
* Received treatment for leishmaniasis including any medication with pentavalent antimony including sodium stibogluconate (Pentostam™), meglumine antimoniate (Glucantime™); amphotericin B (including liposomal amphotericin B and amphotericin B deoxycholate); or other medications containing paromomycin (administered parenterally or topically) or methylbenzethonium chloride (MBCL); gentamicin; fluconazole; ketoconazole; pentamidine; miltefosine, azithromycin or allopurinol that was completed within 56 days of starting study treatments
* History of known or suspected hypersensitivity or idiosyncratic reactions to aminoglycosides
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
2 Years
Study:
NCT01790659
Study Brief:
Protocol Section:
NCT01790659