跳至主要内容
临床试验/ACTRN12617000456358
ACTRN12617000456358已完成4 期

Efficacy and safety of the medications of first line treatment (artesunate+amodiaquine) and second line treatment (artemether+lumefantrine) for the treatment of uncomplicated Plasmodium falciparum in Malabo, Bata and Ebibey, Equatorial Guinee

Ministry of Public Health of Equatorial Guinea0 个研究点目标入组 528 人开始时间: 2017年3月28日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
528

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
6 Months 至 59 Months(—)
性别
All

入选标准

  • 1. age from 6 to 59 months;
  • 2. mono-infection with P. falciparum detected by microscopy;
  • 3. parasitaemia of 1000–200,000/microliter asexual forms;
  • 4. presence of axillary temperature greater or equal to 37.5 degrees C or history of fever during the past 24 h
  • 5. ability to swallow oral medication;
  • 6. ability and willingness to comply with the study protocol for the duration of the study and to comply with the study visit schedule;
  • 7. informed consent from the patient or parent/ guardian of children.

排除标准

  • 1. presence of general danger signs in children aged under 5 years or signs of severe falciparum malaria according to the definitions of WHO;
  • 2. weight under 5 kg;
  • 4. mixed or mono-infection with another Plasmodium species detected by microscopy;
  • 5. presence of severe malnutrition defined as a child aged 6-60 months has a mid-upper arm circumference below 115 mm)
  • 6. presence of febrile conditions due to diseases other than malaria (e.g. measles, acute lower respiratory tract infection, severe diarrhea with dehydration) or other known underlying chronic or severe diseases (e.g. cardiac, renal and hepatic diseases, HIV/AIDS);
  • 7. regular medication, which may interfere with antimalarial pharmacokinetics;
  • 8. history of hypersensitivity reactions or contraindications to any of the medicine(s) being tested or used as alternative treatment(s).

研究者

发起方
Ministry of Public Health of Equatorial Guinea

相似试验

招募中
Unknown
Efficacy and safety of initial treatment (combination immunotherapy or chemotherapy + ICI) in advanced non-small cell lung cancer patients (TPS 1-49%): A multicenter retrospective observational study (TOPGAN2023-01)non small cell carcinoma
JPRN-UMIN000052228department of respiratory medicine hirosaki university graduate school of medicine300
进行中(未招募)
1 期
A Phase I/II Safety, Pharmacodynamic, and Pharmacokinetic Study of Intravenously Administered PXD101 Plus Carboplatin or Paclitaxel or Both in Patients with Advanced Solid Tumours - PXD101-040-EU Global V4In the MTD expansion arm only women with a history of epithelial ovarian, primary peritoneal, fallopian tube or mixed mullerian tumours of ovarian origin participate to confirm the safety and to examine efficacy in this specific patient population.MedDRA version: 8.1 Level: LLT Classification code 10033128 Term: Ovarian cancer
EUCTR2005-002338-36-GBTopoTarget A/S65
已完成
1 期
Safety, efficacy and pharmacokinetic study of paclitaxel injection concentrate for nano-dispersion in subjects with metastatic breast cancer.
CTRI/2009/091/000262Sun Pharma Advanced Research Company Ltd36
招募中
4 期
Clinical trial to compare the effectiveness of migraine’s preventive treatments in primary careMigraine
2024-513597-22-00Institut Universitari D Investigacio En Atencion Primaria Jordi Gol460
尚未招募
不适用
Safety and efficacy on glaucoma treatment with 3 topical medicationsin one bottle x medications in separated bottlesopen angle glaucoma
RBR-6kkmskkcentro oftalmologico de minas gerais
Efficacy and safety of the medications of first line... | 临床试验