Miltefosine efficacy will be \>85%
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
37
2.5 mg/kg/day for 12 weeks
2.5 mg/kg/day for 8 weeks
Institute of Medical Sciences, Banaras Hindu University,
Varanasi, India
Cure rate
Time frame: 12 months after end of treatment
adverse events
gastrointestinal events: vomiting and diarrhea
Time frame: during therapy: the 8 weeks of therapy for the 8 week treatment group and 12 weeks of therapy for the 12 week treatment group
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