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临床试验/NCT00002075
NCT00002075已完成不适用

Multicenter Comparison of Fluconazole (UK-49,858) and Amphotericin B as Treatment for Acute Cryptococcal Meningitis

Pfizer1 个研究点 分布在 1 个国家开始时间: 2001年8月31日最近更新:
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试验速览

阶段
不适用
状态
已完成
发起方
Pfizer
试验地点
1

研究概览

简要总结

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

研究设计

研究类型
Interventional
主要目的
Treatment

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Concurrent Medication:
  • •Immunosuppressant therapy.
  • •Antiviral such as zidovudine.
  • •Radiation therapy for mucocutaneous Kaposi's sarcoma.
  • •Prophylaxis for Pneumocystis carinii pneumonia (PCP) including aerosol pentamidine.
  • •Concurrent Treatment:
  • •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:
  • •Immunosuppressant therapy.
  • •Antivirals such as zidovudine (AZT).
  • •Prophylaxis for Pneumocystis carinii pneumonia (PCP) including aerosol pentamidine.

排除标准

  • •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:
  • •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:
  • •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:
  • •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:
  • •Lymphocyte replacement.

研究者

发起方
Pfizer
申办方类型
Industry

研究点 (1)

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