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临床试验/NCT01775592
NCT01775592已完成4 期

Monitoring the Efficacy of Dihydroartemisinin - Piperaquine in Patients With Uncomplicated Falciparum Malaria in Traleng Commune, Central Vietnam

National Institute of Malariology, Parasitology and Entomology, Vietnam1 个研究点 分布在 1 个国家目标入组 95 人开始时间: 2012年9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
95
试验地点
1
主要终点
Parasite clearance time

研究概览

简要总结

Resistance of Plasmodium falciparum toward Artemisinins, the most important drug for the successful treatment of malaria, has been confirmed in Cambodia. There are few reports from neighbouring countries about delayed parasite rates. The investigators therefore aim to assess parasite clearance in malaria patients in central Vietnam when treated according to national standard guidelines.

详细描述

General objective To evaluate the efficacy of DHA-PPQ in patients with uncomplicated falciparum malaria in a rural area of Central Vietnam, and to assess the in vitro susceptibility of P.falciparum isolates to DHA and PPQ.

Specific objectives

  1. To measure the parasite clearance time in falciparum malaria patients treated with DHA-PPQ.
  2. To determine the efficacy of DHA-PPQ at day 42 post-treatment.
  3. To assess the in vitro susceptibility of P.falciparum isolates towards DHA and PPQ in Quang Nam Province.
  4. To compare genetic profiles of P.falciparum isolates with delayed and those with normal clearance times in order to identify potential markers of resistance;

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
2 Months 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age: from 6 months of age;
  • Fever (body temperature above 37.5C) or history of fever in the previous 24 hours;
  • Mono-infection with P.falciparum with parasite density between 500-100,000/µl
  • Written informed consent to participate to the trial. For patients aged less than 18 years, an informed consent will be obtained from a parent or a guardian.

排除标准

  • Mixed malaria infection;
  • Pregnancy or lactation (urine test for β human chorionic gonadotropin to be performed on any woman of child bearing age unless menstruating);
  • Concomitant acute illness necessitating specific treatment (antibiotics);
  • Underlying chronic severe illness (e.g. cardiac, renal, hepatic diseases, HIV/AIDS).
  • Severe malnutrition;
  • Danger signs:
  • not able to drink
  • incontrollable vomiting
  • recent history of convulsions (>1 in 24 hours)
  • unconscious state; neurological impairment
  • unable to sit or stand
  • Signs of severe malaria:
  • Cerebral malaria (unrousable coma)
  • Severe anaemia (Htc< 15%)
  • Renal failure (serum creatinine > 3 mg/dL)
  • Pulmonary oedema;
  • Hypoglycemia (<40mg/dL)
  • Shock (systolic BP < 70 mmHg in adults, 50 in children)
  • Spontaneous bleeding
  • Repeat generalized convulsions
  • Macroscopic haemoglobinuria
  • Severe jaundice
  • Persons who have received quinine, artemisinin or artemisinin derivatives within the last 7 days, 4-aminoquinolines within the last 14 days, pyrimethamine and/or sulfonamides within the last 28 days, or mefloquine within the last 56 days should be excluded from the in vitro testing

研究组 & 干预措施

Arterakin

Other

Number of DHA- PPQ (Arterakin™) tablets per day at 0hour, 8hours, 24hours, 48hours (according to age): 2 - 3 years:0.5, 0.5, 0.5, 0.5 3 - < 8 years: 1.0, 1.0, 1.0, 1.0 8 - < 15 years:1.5, 1.5, 1.5, 1.5

≥ 15 years:2.0, 2.0, 2.0, 2.0

干预措施: Arterakin (DHA-PPQ) (Drug)

结局指标

主要结局

Parasite clearance time

时间窗: Day 2-5

次要结局

  • efficacy of DHA-PPQ at day 42 post-treatment in Traleng Quangnam, Vietnam(Day 42)
  • in vitro susceptibility of P.falciparum isolates towards DHA and PPQ in Quang Nam Province(Day 3-10)

研究者

发起方
National Institute of Malariology, Parasitology and Entomology, Vietnam
申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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