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临床试验/PER-020-23
PER-020-23尚未招募3 期

Focal mass drug Administration for vivax Malaria Elimination (FLAME): a pragmatic cluster randomized controlled trial in Peru

os Regentes de la Universidad de California0 个研究点目标入组 0 人开始时间: 2024年2月21日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方

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

性别
All

入选标准

  • 1. Eligible to receive CQ and ineligible to receive TQ
  • 2. Age =6 months old
  • 3. Adult =18 years old that provides informed consent
  • 4. A child =8 years and <18 years old that provides informed assent and has informed consent from their parents
  • 5. A child =6 months old and <8 years old that has informed consent from their parents
  • Chloroquine
  • 1. Resides in neighboring household but within 200 m of Pv index case in the past 2 years
  • 2. Age =6 months old
  • 3. Present for intervention
  • 4. Adult =18 years old that provides informed consent
  • 5. A child =8 years and <18 years old that provides informed assent and has informed consent from their parents
  • 6. A child =6 months old and <8 years old that has informed consent from their parents
  • Tafenoquine
  • 1. Eligible to receive CQ
  • 2. Age =16 years old
  • 3. Adult =18 years old that provides informed consent
  • 4. A child =16 years and <18 years old that provides informed assent and has informed consent from their parents

排除标准

  • Chloroquine
  • 1. History of retinal or visual field changes
  • 2. Known hypersensitivity or adverse reaction to CQ
  • 3. Currently taking CQ or have taken CQ in the past four weeks
  • 4. Ineligible for TQ or PQ (see criterio below)
  • 5. Hemoglobin <7 g/dL
  • Tafenoquine
  • 1. G6PD deficiency or intermediate status (defined as activity =6 UI/gHb per SD biosensor)
  • 2. G6PD status unknown or refusal of G6PD status test
  • 3. Acute or severe malaria
  • 4. Pregnancy (known or identified by pregnancy test)
  • 5. Refusal of pregnancy test if new amenorrhea in the past 4 weeks
  • 6. Woman breastfeeding to child that is G6PD deficient or with unknown G6PD status
  • 7. Known hypersensitivity or adverse reaction to TQ or PQ
  • 8. Have taken mefloquine (i.e. artesunate-mefloquine), TQ or PQ, or other antimalarial in the past four weeks
  • 9. Hemoglobin < 7 g/dL
  • 1. G6PD deficiency (defined as activity <4 UI/gHb per SD biosensor)
  • 2. G6PD status unknown or refusal of G6PD status test
  • 3. Acute or severe malaria
  • 4. Pregnancy (known or identified by pregnancy test)
  • 5. Refusal of pregnancy test if new amenorrhea in the past 4 weeks
  • 6. Infant child with G6PD deficiency or unknown G6PD status
  • 7. Known hypersensitivity or adverse reaction to TQ or PQ
  • 8. Have taken mefloquine (i.e. artesunate-mefloquine), TQ or PQ, or other antimalarial in the past four weeks
  • 9. Hemoglobin < 7 g/dL

研究者

发起方
os Regentes de la Universidad de California

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