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临床试验/NCT01380301
NCT01380301终止2 期

Treatment of Bolivian Cutaneous Leishmaniasis With a Combination of Short Courses of Miltefosine and Antimony

Foundation Fader1 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2007年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
发起方
入组人数
19
试验地点
1
主要终点
Healing of ulcers

研究概览

简要总结

Cutaneous leishmaniasis is endemic in the New World and, until recently, the standard treatment was pentavalent antimony. The cure rate for L panamensis in Colombia is 91%-93% and the cure rate in Bolivia is also 90%. Nevertheless, pentavalent antimonials have the disadvantages of multiple injections and mild-moderate clinical toxicity all of which are particularly unpleasant for a moderate clinical problem such as cutaneous leishmaniasis.

The oral agent Miltefosine has now been shown to be as effective as antimony in Colombia and Bolivia (91 and 92% respectively). Side effects seen in patients with cutaneous disease that can be specifically attributed to the drug are nausea and vomiting of mild grade in approximately 25% of patients, and low-grade elevation of creatinine also in approximately 25% of patients. A further disadvantage of miltefosine is that regimens shorter than 4 weeks have not been evaluated for cutaneous disease.

Combination therapy is now being used for many infectious diseases, such as tuberculosis, malaria, and HIV. Combination therapy offers the potential of preventing drug resistance, because organisms resistant to one of the drugs may be susceptible to the other drug; and also the potential to diminish drug therapy duration and thus side effects. These two potential benefits to some extent contradict each other: preventing resistance is best done if full courses of both drugs is used; diminishing therapy duration means using less than the full course of each drug. The optimum combination regimen is one in which sufficient amounts of both drugs are used to have high efficacy, yet the amounts are as low as possible to spare patients unnecessarily long courses of drug.

In the present protocol, the combination of a half-course of miltefosine and a half-course of antimony will be evaluated for efficacy and tolerance. The combination of miltefosine and antimony is chosen because these are now the two standard agents in Bolivia, and in vitro the combination was additive to mildly synergistic against a standard leishmania strain.

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
12 Years 至 75 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Parasitological confirmation
  • at least 1 lesion must be ulcerative
  • No specific antileishmanial therapy during the previous six months

排除标准

  • Concomitant diseases such as Tuberculosis, HIV, diabetes, renal failure, liver disease
  • abnormalities CTC 2 in blood, liver, kidney test or EKG

研究组 & 干预措施

Miltefosine and Antimony

Experimental

Miltefosine 1,5 to 2,5 mg x k x d during 14 days simultaneously with meglumine antimoniate 20 mg x kg x d during 10 days

干预措施: Miltefosine and antimony (Drug)

Miltefosine alone

Active Comparator

Miltefosine 1,5 to 2,5 mg x kg x d during 14 days

干预措施: Miltefosine alone (Drug)

结局指标

主要结局

Healing of ulcers

时间窗: 45 days

次要结局

  • Clinical findings and Laboratory parameters in normal ranges(28 days)

研究者

发起方
Foundation Fader
申办方类型
Other

研究点 (1)

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