NCT Number: NCT00002019
Safety and Efficacy of Amphotericin B Lipid Complex in the Treatment of Cryptococcal Meningitis in Patients With the Acquired Immunodeficiency Syndrome
To evaluate the safety, tolerance and efficacy of three different dosage regimens of Amphotericin B Lipid Complex (ABLC) compared to Fungizone (Amphotericin B) in patients with AIDS and cryptococcal meningitis.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
Harbor - UCLA Med Ctr, Torrance, California, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Concurrent Medication:
Allowed:
- Intravenous pentamidine for treatment of Pneumocystis carinii pneumonia (PCP) but not for prophylaxis.
Patients must have the following:
- Meet the CDC criteria for diagnosis of AIDS.
- Confirmed episode of acute cryptococcal meningitis.
- Informed consent of the patient or guardian prior to entry.
Exclusion criteria
Co-existing Condition:
Patients with the following conditions or symptoms are excluded:
- Clinical evidence of acute or chronic meningitis due to an agent other than Cryptococcus neoformans.
- History of hypersensitivity/anaphylactoid reaction attributed to amphotericin B.
- Any other concomitant condition which, in the opinion of the investigator, would preclude a patient's participation in the study.
Concurrent Medication:
Excluded:
- Corticosteroids.
- Salicylates or other drugs known to interfere with prostaglandin synthesis except as specified in protocol.
- Zidovudine.
- Investigational agents.
- Interferon.
- Interleukin-2 (IL-2).
- Steroids.
- Isoprinosine.
- Intrathecal Amphotericin B.
- Intravenous Pentamidine PCP prophylaxis (only treatment).
Patients with the following are excluded:
- Clinical evidence of acute or chronic meningitis due to an agent other than Cryptococcus neoformans.
- History of hypersensitivity/anaphylactoid reaction attributed to amphotericin B.
- Inability to obtain appropriate follow-up visits.
- Any other concomitant condition which, in the opinion of the investigator, would preclude a patient's participation in the study.
Prior Medication:
Excluded within 4 weeks of study entry:
- Amphotericin B.
- Excluded within 2 weeks of study entry:
- Any other experimental drug.
Treatment and study plan
Amphotericin B
DrugSponsors and collaborators
Lead sponsor
Liposome
Industry
Registry information
Important dates
- First posted
- Aug 31, 2001
- Registry last updated
- Jun 24, 2005
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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