Randomized, Controlled, Double-Blind Study of Itraconazole Oral Solution Versus Fluconazole Tablets for the Treatment of Esophageal Candidiasis.
This study has been completed.
Sponsor:
Janssen, LP
Information provided by:
NIH AIDS Clinical Trials Information Service
ClinicalTrials.gov Identifier:
NCT00002132
First received: November 2, 1999
Last updated: June 23, 2005
Last verified: April 1996
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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 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety Study Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | Randomized, Controlled, Double-Blind Study of Itraconazole Oral Solution Versus Fluconazole Tablets for the Treatment of Esophageal Candidiasis. |
Resource links provided by NLM:
Further study details as provided by NIH AIDS Clinical Trials Information Service:
Eligibility| Ages Eligible for Study: | 13 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria
Patients must have:
- Esophageal candidiasis.
- Histological evidence of Candida spp. at baseline with confirmation by positive mycological culture.
- HIV infection or other predisposing risk factor.
- Life expectancy of at least 2 months.
Exclusion Criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
- Malignancies of the head or neck, if the treatment or disease will interfere with response assessment.
- Evidence of systemic fungal infection.
- Underlying clinical condition that would preclude study completion.
- Judged to be unreliable in regard to following physician's directives.
Concurrent Medication:
Excluded:
- Rifampin.
- Rifabutin.
- Phenobarbital.
- Phenytoin.
- Carbamazepine.
- Terfenadine.
- Astemizole.
- H2 blockers.
- Continual antacids.
- Any investigational drug (expanded access drugs are allowed).
Patients with the following prior conditions are excluded:
- History of significant hepatic abnormalities or clinical evidence of hepatic disease within 2 months prior to study entry.
- History of hypersensitivity to imidazole or azole compounds.
Prior Medication:
Excluded:
- Other orally administered antifungal therapy within 3 days prior to study entry.
- Any investigational drug within 1 month prior to study entry (expanded access drugs are allowed).
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00002132
Locations
| United States, Arizona | |
| Dr Eskild A Petersen | |
| Tucson, Arizona, United States, 85724 | |
| United States, California | |
| Los Angeles County - USC Med Ctr | |
| Los Angeles, California, United States, 90033 | |
| UCSD Med Ctr | |
| San Diego, California, United States, 92103 | |
| 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 | |
| Erie County Med Ctr | |
| Buffalo, New York, United States, 14215 | |
| Dr Douglas Dieterich | |
| New York, New York, United States, 10016 | |
| 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 | |
Sponsors and Collaborators
Janssen, LP
More Information
Publications:
| ClinicalTrials.gov Identifier: | NCT00002132 History of Changes |
| Other Study ID Numbers: | 236A, ITR-USA-12 |
| Study First Received: | November 2, 1999 |
| Last Updated: | June 23, 2005 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by NIH AIDS Clinical Trials Information Service:
|
Itraconazole Fluconazole Acquired Immunodeficiency Syndrome Candidiasis Immunocompromised Host |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Candidiasis Esophageal Diseases Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases |
Mycoses Gastrointestinal Diseases Digestive System Diseases Fluconazole Itraconazole Hydroxyitraconazole Antifungal Agents Anti-Infective Agents Therapeutic Uses Pharmacologic Actions 14-alpha Demethylase Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action |
ClinicalTrials.gov processed this record on May 16, 2013