A Phase 2 interventional study of azithromycin plus artesunate and Artesunate in Uncomplicated Falciparum Malaria, sponsored by Medical University of Vienna. Completed at 1 site in Bangladesh. Open to participants aged 8 Years to 65 Years. Per ClinicalTrials.gov, last updated 2012-11-01.
Sponsored by Medical University of Vienna · Phase 2, Interventional, and Treatment
The purpose of this study is to investigate the efficacy of azithromycin combination therapy with artesunate for the treatment of uncomplicated falciparum malaria in Bangladesh.
In view of spreading antimalarial drug resistance there is an urgent need for new combination treatments for a disease that kills more than one million people every year. Azithromycin is a macrolide antibiotic that is particularly attractive due to its safety in children and experience with use in pregnancy. Recent trials suggest that azithromycin has a strong potential as an antimalarial. The purpose of this study is to investigate the efficacy of azithromycin combination therapy for the treatment of uncomplicated falciparum malaria in Bangladesh.
1,299 studies on the registry are indexed under Malaria; 86 are open to participants now.
This study's enrollment of 228 is close to the median of 220 across 1,027 interventional studies indexed under Malaria.
Browse Malaria studies →Medical University of Vienna is the lead sponsor of 1,076 studies on the registry; 177 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Azithromycin + Artesunate treatment
Drug: azithromycin plus artesunate
Artesunate treatment controls
Drug: Artesunate
Primary clinical outcome is cure (ACPR as defined by WHO criteria) on Day 42.
Time frame: 42 days
Secondary outcome measures are time until parasite, fever, and gametocyte clearance (PCT, FCT, and GCT).
Time frame: 42
This study is completed, as verified in Oct 2012. You cannot join it, but the record below documents what was studied.
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Medical University of Vienna