跳至主要内容
临床试验/NCT00002068
NCT00002068已完成不适用

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

Pfizer8 个研究点 分布在 2 个国家开始时间: 2001年8月31日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Pfizer
试验地点
8

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
13 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Concurrent Medication:
  • •Immunosuppressant therapy.
  • •Antiviral therapy such as zidovudine.
  • •Prophylaxis for Pneumocystis carinii pneumonia.
  • •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.
  • •Antiviral therapy such as zidovudine.
  • •Prophylaxis for Pneumocystis carinii pneumonia.

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.
  • •Concurrent Medication:
  • •Excluded within 4 weeks of study entry:
  • •Greater than 1 mg/kg/wk amphotericin B.
  • •Coumadin-type anticoagulants.
  • •Oral hypoglycemics.
  • •Barbiturates.
  • •Phenytoin.
  • •Immunostimulants.
  • •Investigational drugs or approved (licensed) drugs for investigational indications.
  • •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:
  • •Excluded within 4 weeks of study entry:
  • •Greater than 1 mg/kg/wk amphotericin B.
  • •Coumadin-type anticoagulants.
  • •Oral hypoglycemics.
  • •Barbiturates.
  • •Phenytoin.
  • •Immunostimulants.
  • •Investigational drugs or approved (licensed) drugs for investigational indications.
  • •Prior Treatment:
  • •Lymphocyte replacement.

研究者

发起方
Pfizer
申办方类型
Industry

研究点 (8)

Loading locations...

相似试验