JPRN-jRCTs071180093招募中2 期
Efficacy and safety of pyrimethamine/sulfadiazine/folinate combination therapy for the treatment of congenital toxoplasmosis - Treatment of congenital toxoplasmosis with pyrimethamine/sulfadiazine
Maruyama Haruhiko0 个研究点目标入组 35 人开始时间: 2019年3月29日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 35
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
- ot applicable 至 ot applicable（—）
- 性别
- All
入选标准
- •1. Confirmed toxoplasmosis fulfilling one of the followings
- •#1 Toxoplasma DNA detected in placenta or other tissues
- •#2 pathological identification of Toxoplasma
- •#3 anti-Toxoplasma IgM in cord blood or sera within 6 months after birth
- •#4 increase of anti-Toxoplasma IgG within 1 year after birth
- •#5 positive anti-Toxoplasma IgG after 12 months after birth
- •2. Suspected toxoplasmosis with all of the followings
- •#1 typical symptoms (e.g. intra-cranial calcification)
- •#2 positive anti-Toxoplasma IgG
- •#3 other congenital infections excluded
排除标准
- •#1 HIV positive patients
- •#2 patients allergic to test compounds
- •#3 patients with megaloblastic anemia due to
- •folate deficiency
- •#4 No consent is given from the patient
- •him/herself nor a legally authorized
- •representative/guardian of the patient
- •#5 patients principal investigator judged
- •inappropriate
研究者
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