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| Sponsored by: |
Janssen, LP |
| Information provided by: | NIH AIDS Clinical Trials Information Service |
| ClinicalTrials.gov Identifier: | NCT00002132 |
Purpose
To evaluate the safety and efficacy of itraconazole oral solution versus fluconazole tablets for the treatment of esophageal candidiasis in immunocompromised patients.
| Condition | Intervention |
|
Candidiasis, Esophageal HIV Infections |
Drug: Itraconazole Drug: Fluconazole |
| MedlinePlus related topics: | AIDS Esophagus Disorders Yeast Infections |
| Drug Information available for: | Itraconazole Fluconazole |
| Study Type: | Interventional |
| Study Design: | Treatment, Double-Blind, Safety Study |
| Official Title: | Randomized, Controlled, Double-Blind Study of Itraconazole Oral Solution Versus Fluconazole Tablets for the Treatment of Esophageal Candidiasis. |
Eligibility
| Ages Eligible for Study: | 13 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria
Patients must have:
Exclusion Criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
Concurrent Medication:
Excluded:
Patients with the following prior conditions are excluded:
Prior Medication:
Excluded:
Contacts and Locations| United States, Arizona | |||||
| Dr Eskild A Petersen | |||||
| Tucson, Arizona, United States, 85724 | |||||
| United States, California | |||||
| UCSD Med Ctr | |||||
| San Diego, California, United States, 92103 | |||||
| Los Angeles County - USC Med Ctr | |||||
| Los Angeles, California, United States, 90033 | |||||
| United States, District of Columbia | |||||
| George Washington Univ Med Ctr | |||||
| Washington, District of Columbia, United States, 20037 | |||||
| United States, Georgia | |||||
| Emory Univ School of Medicine | |||||
| Atlanta, Georgia, United States, 30303 | |||||
| United States, Illinois | |||||
| Rush Presbyterian - Saint Luke's Med Ctr | |||||
| Chicago, Illinois, United States, 60612 | |||||
| United States, Maryland | |||||
| Johns Hopkins Univ School of Medicine | |||||
| Baltimore, Maryland, United States, 21205 | |||||
| United States, Michigan | |||||
| Wayne State Univ / Harper Hosp | |||||
| Detroit, Michigan, United States, 48201 | |||||
| United States, Missouri | |||||
| Univ of Missouri at Kansas City School of Medicine | |||||
| Kansas City, Missouri, United States, 64108 | |||||
| Infectious Diseases Association / Research Med Ctr | |||||
| Kansas City, Missouri, United States, 64132 | |||||
| United States, New York | |||||
| Montefiore Med Ctr | |||||
| Bronx, New York, United States, 10467 | |||||
| Dr Douglas Dieterich | |||||
| New York, New York, United States, 10016 | |||||
| Erie County Med Ctr | |||||
| Buffalo, New York, United States, 14215 | |||||
| United States, North Carolina | |||||
| Univ of North Carolina | |||||
| Chapel Hill, North Carolina, United States, 27599 | |||||
| Bowman Gray School of Medicine | |||||
| Winston Salem, North Carolina, United States, 27157 | |||||
| United States, Ohio | |||||
| Univ Hosps of Cleveland | |||||
| Cleveland, Ohio, United States, 44106 | |||||
| United States, Texas | |||||
| Austin Infectious Disease Consultants | |||||
| Austin, Texas, United States, 78705 | |||||
| Houston Veterans Administration Med Ctr | |||||
| Houston, Texas, United States, 77030 | |||||
| Janssen, LP |
More Information
| Study ID Numbers: | 236A, ITR-USA-12 |
| First Received: | November 2, 1999 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00002132 |
| Health Authority: | United States: Food and Drug Administration |
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