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临床试验/NCT01032187
NCT01032187已完成4 期

Efficacy and Safety of Amphotericin B Deoxycholate Compared to Meglumine Antimoniate for Treatment of Visceral Leishmaniasis in Brazilian Children

University of Brasilia2 个研究点 分布在 1 个国家目标入组 101 人开始时间: 2007年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
101
试验地点
2
主要终点
Cure rate

研究概览

简要总结

The purpose of this study is to determine if amphotericin B is effective against visceral leishmaniasis in Brazilian children. Amphotericin B will be compared to meglumine antimoniate which is the current approved drug used for this disease in Brazil.

详细描述

Despite their high toxicity, antimonials and amphotericin B deoxycholate are commonly used for treating visceral leishmaniasis (VL). Few studies showing conflictive data about their efficacy and adverse events in pediatric population are available. This study aimed to evaluate efficacy and safety of amphotericin B deoxycholate vs. that of N-methylglucamine antimoniate in treating pediatric VL in Brazil. This was a randomized, open-label, 2-arm and controlled pilot clinical trial. Treatment naïve children and adolescents with VL without signs of severe illness were treated with N-methylglucamine antimoniate or amphotericin B deoxycholate. All patients were diagnosed with positive direct examination and/or positive PCR for Leishmania spp. performed in bone marrow samples. The primary efficacy end-point was VL cure determined after 180 days of completion of treatment. The analysis was performed using intention-to-treat (ITT) and per protocol (PP) analyses.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
6 Months 至 12 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Clinical symptoms of visceral leishmaniasis: fever plus hepatomegaly or splenomegaly
  • Diagnosis of visceral leishmaniasis confirmed through parasite visualization in bone marrow smears or positive serology (indirect immunofluorescent antibody test or rK39 rapid test)or positive kDNA PCR test

排除标准

  • Any of the following laboratory findings
  • Total serum bilirubin higher than 2,5 mg/dL
  • Serum SGOT higher than 5 times the upper normal level
  • Serum SGPT higher than 5 times the upper normal level
  • Prothrombin time concentration lower than 70%
  • Abnormal serum creatinine
  • Any of the following signs or symptoms
  • Generalized edema
  • Severe malnutrition
  • Systemic inflammatory response syndrome
  • Any of the following conditions
  • HIV infection/disease
  • Corticoid or immunosuppressive drugs use
  • Symptomatic heart diseases
  • Chronic hepatic or renal diseases
  • Lupus erythematosus

研究组 & 干预措施

Meglumine antimoniate

Active Comparator

20mg/kg/day IV for 20 days

干预措施: Meglumine antimoniate (Drug)

Anfo B

Experimental

Amphotericin B-deoxycholate, 1mg/kg/day IV for 14 days

干预措施: Amphotericin B-deoxycholate (Drug)

结局指标

主要结局

Cure rate

时间窗: 3 months

次要结局

  • Adverse events rate(30 days)
  • Improvement rate(30 days)

研究者

发起方
University of Brasilia
申办方类型
Other
责任方
Principal Investigator
主要研究者

Gustavo Adolfo Sierra Romero

Associate Professor

University of Brasilia

研究点 (2)

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