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OBJECTIVES: I. Identify a preferred oral fluconazole dose regimen for patients with non-acute histoplasmosis or blastomycosis, or ulcerocutaneous or deep sporotrichosis. II. Study the safety and effi...
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Lead Sponsor
National Center for Research Resources (NCRR)
Collaborators
NCT04059770 · Histoplasmosis, AIDS
NCT06523998 · Sporotrichosis, Chromomycosis, and more
NCT05685641 · Acquired Immunodeficiency Syndrome, Histoplasmosis AIDS, and more
NCT02911740 · Tuberculosis, HIV, and more
NCT00001702 · Blastomycosis
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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