CTIS2024-515968-32-00进行中（未招募）1 期
Randomized non-inferiority clinical trial to evaluate the efficacy of a single fixed dose of 18 mg ivermectin for the treatment of uncomplicated strongyloidiasis. - STRONG-FIX
Fundacio Hospital Universitari Vall D’Hebron Institut De Recerca0 个研究点目标入组 276 人开始时间: 2024年7月15日最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 276
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 65+（—）
- 性别
- All
入选标准
- •Age equal to or greater than 18 years., Signature of the informed consent., Diagnosis of strongyloidiasis either by direct parasitological methods (detection of larvae in coproparasitology or in the specific Strongyloides culture) or by positivity of a serological technique (ELISA) with an optical density index (OD) greater than or equal to 2., Current residence in an area with no evidence of active transmission of strongyloidiasis.
排除标准
- •Pregnancy or lactation, Intolerance or allergy to ivermectin., Presence of any condition that implies immunosuppression (both due to drugs and underlying disease): treatment with corticosteroids at a dose greater than or equal to 20 mg/day for more than 14 days, treatment with cytotoxic or antimetabolites, bone marrow transplantation or Solid organ failure, biologic drugs, active solid or hematologic neoplasm, hypogammaglobulinemia, HIV infection with a CD4 count less than 200 cells/mm3., Kidney failure (glomerular filtration rate equal to or less than 30 ml/min) or advanced liver disease (Child B or C)., Loa loa co-infection (due to risk of encephalopathy when administering ivermectin).
研究者
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