跳至主要内容
临床试验/PACTR202402822223203
PACTR202402822223203尚未招募4 期

Assessment of combined antiparasitic drugs praziquantel and albendazole versus albendazole alone in the treatment of active parenchymal neurocysticercosis in Tanzania and Zambia.

REvolution Worldwide S.r.l. Impresa Sociale0 个研究点目标入组 300 人开始时间: 2024年1月31日最近更新:
适应症

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
300

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
19 Year(s) 至 44 Year(s)(—)
性别
All

入选标准

  • Inclusion for screening:
  • Living in the study area for a continuous period of 3 years
  • Late onset/acquired epilepsy
  • Adult aged 18 years and above
  • Are willing and able to consent to this study
  • Are willing to undergo diagnostic procedures
  • Inclusion criteria for the treatment study:
  • Adult aged 18 years and above
  • Are willing and able to consent to this study
  • Meet the definitions of active symptomatic NCC
  • Have late onset of epilepsy or history of seizures, epileptic seizures
  • Are willing to undergo diagnostic procedures
  • Are medically stable enough for trial medication to be initiated
  • Are willing to be hospitalized for 11-20 days to receive treatment for NCC
  • Are willing to be followed up for one year following receipt of study medication

排除标准

  • The participants will be excluded if;
  • Are pregnant or breastfeeding
  • Symptomatic NCC with cysts in extra-parenchymal location (sub-arachnoid and/or ventricles)
  • Have uncontrolled hypertension and/or diabetes
  • Have chronic consuming illness such as cancer or mental handicap to not allow them to follow the study instructions
  • Have severe immunodeficiency eg. HIV/AIDS or Autoimmune diseases
  • Already known allergies to albendazole
  • Subject taking part in another clinical/pharmacological study in the 30 days preceding enrollment

研究者

发起方
REvolution Worldwide S.r.l. Impresa Sociale

相似试验