ClinicalTrials.gg
CompletedNCT00002305Updated Jun 24, 2005

A Comparison of Fluconazole and Amphotericin B in the Treatment of Cryptococcal Meningitis

An interventional study of Flucytosine and Fluconazole in Meningitis, Cryptococcal and HIV Infections, sponsored by Pfizer. Completed at 45 sites in 2 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2005-06-24.

Sponsored by Pfizer · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Ages
18 Years and older
Sex
All
01

Study summary

To compare the safety and effectiveness of fluconazole and amphotericin B, alone or in combination with flucytosine, as treatment for acute cryptococcal meningitis.

02

Conditions studied

  • Meningitis, Cryptococcal
  • HIV Infections

Keywords

  • AIDS-Related Opportunistic Infections
  • Meningitis
  • Cryptococcosis
  • Drug Therapy, Combination
  • Fluconazole
  • Flucytosine
  • Acquired Immunodeficiency Syndrome
  • Amphotericin B
03

In context

Meningitis, Cryptococcal

54 studies on the registry are indexed under Meningitis, Cryptococcal; 6 are open to participants now.

Browse Meningitis, Cryptococcal studies →

Lead sponsor

Pfizer is the lead sponsor of 3,334 studies on the registry; 149 are open to participants now.

Of its 601 completed or terminated interventional studies of FDA-regulated products, 391 (65%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Concurrent Medication:

Allowed:

  • therapy.
  • Antiviral therapy such as zidovudine.
  • Prophylaxis for Pneumocystis carinii pneumonia.

Concurrent Treatment:

Allowed:

  • Radiation therapy for mucocutaneous Kaposi's sarcoma.

Written 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.
  • Antiviral therapy (such as zidovudine).
  • Prophylaxis for Pneumocystis carinii pneumonia.

Exclusion criteria

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.
  • 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:
  • Greater 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:
  • Greater than 1 mg/kg/wk amphotericin B.

Prior Treatment:

Excluded:

  • Lymphocyte replacement.
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

05

Study design

Phase
Not applicable
Primary purpose
Treatment

Interventions

06

Study locations

45 sites
  • Univ of Alabama at Birmingham
    Birmingham, Alabama 35294, United States
  • Tucson Veterans Administration Med Ctr
    Tucson, Arizona 85724, United States
  • UCLA CARE Ctr
    Los Angeles, California 90095, United States
  • Dr Shelly Gordon
    San Francisco, California 94115, United States
  • Dr Martin Mass
    San Francisco, California 94120, United States
  • Dr Paul Rothman
    Sherman Oaks, California 91403, United States
  • Christiana Hosp / Med Ctr of Delaware
    Wilmington, Delaware 19899, United States
  • George Washington Univ Med Ctr
    Washington, District of Columbia 20037, United States
  • Univ of Miami School of Medicine
    Miami, Florida 331361013, United States
  • Univ of South Florida
    Tampa, Florida 33612, United States
  • Emory Univ School of Medicine
    Atlanta, Georgia 30303, United States
  • Med College of Georgia
    Augusta, Georgia 30912, United States
  • DeKalb Gen Hosp
    Decatur, Georgia 30033, United States
  • Northwestern Univ Med School
    Chicago, Illinois 60611, United States
  • Louisiana State Univ School of Medicine
    New Orleans, Louisiana 70112, United States
  • Tulane Univ School of Medicine
    New Orleans, Louisiana 70112, United States
  • Dr Michael Bach
    Portland, Maine 04102, United States
  • Univ of Maryland / Inst of Human Virology
    Baltimore, Maryland 212011192, United States
  • Loch Raven Veterans Hosp
    Baltimore, Maryland 21218, United States
  • New England Med Ctr
    Boston, Massachusetts 02111, United States
  • Univ Hosp
    Boston, Massachusetts 02118, United States
  • Ann Arbor Veterans Administration Med Ctr
    Ann Arbor, Michigan 48105, United States
  • Harper Hosp
    Detroit, Michigan 48201, United States
  • Henry Ford Hosp
    Detroit, Michigan 48202, United States
  • Washington Univ School of Medicine
    St. Louis, Missouri 63108, United States
  • Albany Med College / AIDS Treatment Ctr
    Albany, New York 12203, United States
  • Montefiore Med Ctr / Bronx Municipal Hosp
    Bronx, New York 10467, United States
  • Bronx Veterans Administration / Mount Sinai Hosp
    Bronx, New York 10468, United States
  • Jewish Hosp Ctr Affiliation
    Jamaica, New York 11432, United States
  • Chelsea Village Med Ctr
    New York, New York 10014, United States
  • Mem Sloan - Kettering Cancer Ctr
    New York, New York 10021, United States
  • Saint Luke's - Roosevelt Hosp Ctr
    New York, New York 10025, United States
  • Columbia Univ
    New York, New York 10032, United States
  • Harlem AIDS Treatment Group / Harlem Hosp Ctr
    New York, New York 10037, United States
  • Univ of North Carolina School of Medicine
    Chapel Hill, North Carolina 275997215, United States
  • Cincinnati Veterans Adm Med Ctr / Univ Hosp
    Cincinnati, Ohio 452670405, United States
  • Ohio State Univ Hosp
    Columbus, Ohio 43210, United States
  • Univ of Tennessee
    Memphis, Tennessee 38163, United States
  • Dr Daniel Barbaro
    Dallas, Texas 75235, United States
  • Univ TX Galveston Med Branch
    Galveston, Texas 77550, United States
  • United States Air Force Med Ctr
    Lackland Air Force Base, Texas 782365300, United States
  • Univ TX San Antonio Health Science Ctr
    San Antonio, Texas 78284, United States
  • Richmond AIDS Consortium
    Richmond, Virginia 23219, United States
  • CHG-118 Group Health / Cooperative of Puget Sound
    Seattle, Washington 98112, United States
  • Saint Michael's Hosp
    Toronto, Ontario, Canada
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 24, 2005, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00002305
Lead sponsor
Pfizer
First posted
Aug 31, 2001
Last update
Jun 24, 2005
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 1989. You cannot join it, but the record below documents what was studied.

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Studies of the drugs tested here: Fluconazole · Amphotericin B

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