Randomised clinical trial comparing oral miltefosine associated with pentoxifylline to intravenous liposomal amphotericin b for the treatment of cutaneous and mucosal leishmaniasis
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
100
Hospital Universitario de Brasilia
Brasília, Federal District, Brazil
RECRUITINGCure
Complete healing of all lesions (cicatrization of ulcers and complete regression of erythema or infiltration)
Time frame: 90 days after the begin of treatment
Adverse effects
Presence laboratorial or clinica changes during treatment that lead to treatment interruption
Time frame: 30 days after drug interruption
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