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Sponsors and Collaborators: |
National Institute of Allergy and Infectious Diseases (NIAID) University of Alabama at Birmingham |
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Information provided by: | Office of Rare Diseases (ORD) |
ClinicalTrials.gov Identifier: | NCT00004938 |
OBJECTIVE:
I. Evaluate the efficacy of fluconazole in patients with lymphocutaneous or visceral sporotrichosis.
Condition | Intervention | Phase |
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Sporotrichosis |
Drug: fluconazole |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Efficacy Study |
Ages Eligible for Study: | 12 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
PROTOCOL ENTRY CRITERIA:
--Disease Characteristics-- Presumptive evidence of sporotrichosis Culture-proven sporotrichosis determined on study Relapsing disease following antifungal therapy eligible if culture positive for Sporothrix schenckii prior to entry No life-threatening disease No central nervous system sporotrichosis --Prior/Concurrent Therapy-- No concurrent drugs known to react with fluconazole No more than 3 days of systemic antifungals for current sporotrichosis episode --Patient Characteristics-- Hepatic: Liver function tests no greater than 5 times normal Other: No HIV infection No pregnant or nursing women
Study ID Numbers: | 199/11815, NIAID-MSG-11815 |
Study First Received: | February 24, 2000 |
Last Updated: | June 8, 2006 |
ClinicalTrials.gov Identifier: | NCT00004938 |
Health Authority: | United States: Federal Government |
fungal infection rare disease sporotrichosis |
Fluconazole Mycoses Skin Diseases, Infectious Skin Diseases Clotrimazole |
Miconazole Tioconazole Rare Diseases Sporotrichosis Dermatomycoses |
Anti-Infective Agents Therapeutic Uses Antifungal Agents Infection Pharmacologic Actions |