A randomized controlled trial to assess the safety and efficacy of azithromycin combination therapy for use in severe malaria. This pilot trial will be conducted in uncomplicated malaria patients in southeastern Bangladesh.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
75
Artesunate alone
Combination of azithromycin + artesunate
MARIB
Bāndarban, Bangladesh
Safety and Tolerability (Number of Participants with Adverse Events)
Time frame: 42 days
Adequate Clinical and Parasitological Response (ACPR) on Days 28 and 42
Time frame: 42 days
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