Meningitis |
bacterial and viral |
Clinical Trial: Multicenter Comparison of Fluconazole (UK-49,858) and Amphotericin B as Treatment for Acute Cryptococcal Meningitis
This study has been completed.
|
Purpose
To compare the safety and effectiveness of fluconazole and amphotericin B, alone or in combination with flucytosine, as treatment for acute cryptococcal meningitis.
| Condition | Treatment or Intervention |
|---|---|
| Meningitis, Cryptococcal HIV Infections | Drug: Flucytosine Drug: Fluconazole Drug: Amphotericin B |
MedlinePlus related topics: AIDS; Fungal Infections; Meningitis; Neurologic Diseases
Study Type: Interventional
Study Design: Treatment
Eligibility
Ages Eligible for Study: 18 Years and above, Genders Eligible for Study: Both
Criteria
Inclusion Criteria
Concurrent Medication: Allowed:
- Immunosuppressant therapy.
- Antiviral such as zidovudine.
- Radiation therapy for mucocutaneous Kaposi's sarcoma.
- Prophylaxis for Pneumocystis carinii pneumonia (PCP) including aerosol pentamidine.
Concurrent Treatment: Allowed:
- Radiation therapy for mucocutaneous Kaposi's sarcoma.
Written informed consent must be obtained for each patient, either from the patient himself or from the patient's legal guardian.
- No prior systemic antifungal therapy for cryptococcosis.
- Relapse after prior therapy.
- Success of prior therapy must have been documented by negative cerebrospinal fluid (CSF) culture at the end of therapy. Following prior therapy, such patients may not have received more than 1 mg/kg/wk amphotericin B in the 4 weeks before entry into study.
Prior Medication: Allowed:
- Immunosuppressant therapy.
- Antivirals such as zidovudine (AZT).
- Prophylaxis for Pneumocystis carinii pneumonia (PCP) including aerosol pentamidine.
Exclusion Criteria
Co-existing Condition: Patients with the following are excluded:
- Evidence of acute or chronic meningitis based upon any etiology other than cryptococcosis.
- History of allergy to or intolerance of imidazoles, azoles, or amphotericin B.
- Moderate or severe liver disease.
- Comatose.
- Unlikely to survive more than 2 weeks.
- Any exceptions to these prohibitions of concomitant medications must be approved by Pfizer Central Research.
Concurrent Medication: Excluded:
- Coumadin-type anticoagulants.
- Oral hypoglycemics.
- Barbiturates.
- Phenytoin.
- Immunostimulants.
- Investigational drugs or approved (licensed) drugs for investigational indications.
- Any exceptions to these prohibitions of concomitant medications must be approved by Pfizer Central Research.
- Excluded within 4 weeks of study entry:
- Received more than 1 mg/kg/wk amphotericin B.
Concurrent Treatment: Excluded:
- Lymphocyte replacement.
Patients with the following are excluded:
- Evidence of acute or chronic meningitis based upon any etiology other than cryptococcosis.
- History of allergy to or intolerance of imidazoles, azoles, or amphotericin B.
- Moderate or severe liver disease.
- Comatose.
- Unlikely to survive more than 2 weeks.
Prior Medication: Excluded:
- Coumadin-type anticoagulants.
- Oral hypoglycemics.
- Barbiturates.
- Phenytoin.
- Immunostimulants.
- Investigational drugs or approved (licensed) drugs for investigational indications.
- Excluded within 4 weeks of study entry:
- More than 1 mg/kg/wk amphotericin B.
Prior Treatment: Excluded:
- Lymphocyte replacement.
Location Information
California
Dr Robert Larsen, Los Angeles, California, 90033, United States
More Information
Record last reviewed: September 1989
Last Updated: October 13, 2004
Record first received: November 2, 1999
ClinicalTrials.gov Identifier: NCT00002075
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005
Resources
- Arachnoiditis (National Institute of Neurological Disorders and Stroke)
- Bacterial Meningitis (Cleveland Clinic)

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