An interventional study of paromomycin and streptomycin in Tuberculosis, Pulmonary, sponsored by FDA Office of Orphan Products Development. Completed. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2015-03-25.
Sponsored by FDA Office of Orphan Products Development · Not applicable, Interventional, and Treatment
OBJECTIVES: I. Compare the pharmacokinetics and early bactericidal activity of paromomycin (aminosidine) vs streptomycin for the treatment of uncomplicated pulmonary tuberculosis.
II. Compare the tolerability of these two drugs in these patients. III. Establish the relationships between achieved serum concentration, minimal inhibitory concentration, and early bactericidal activity of paromomycin and streptomycin.
PROTOCOL OUTLINE: This is a randomized study. Patients are randomized to one of three treatment arms. Patients in arms I and II receive one of two doses of paromomycin intramuscularly once a day for 3 days. Patients in arm III receive streptomycin intramuscularly once a day for 3 days. All patients then begin a course of standard therapy for tuberculosis.
1,417 studies on the registry are indexed under Tuberculosis; 208 are open to participants now.
This study's enrollment of 24 is below the median of 150 across 952 interventional studies indexed under Tuberculosis.
Browse Tuberculosis studies →FDA Office of Orphan Products Development is the lead sponsor of 31 studies on the registry; none are open to participants now.
Counted across the registry records on this site, refreshed daily.
PROTOCOL ENTRY CRITERIA:
--Disease Characteristics--
--Prior/Concurrent Therapy--
--Patient Characteristics--
No study locations are listed for this record.
This study is completed, as verified in Feb 2001. You cannot join it, but the record below documents what was studied.
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FDA Office of Orphan Products Development