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临床试验/JPRN-jRCTs031190157
JPRN-jRCTs031190157进行中(未招募)2 期

Clinical study on the safety of sirolimus for epileptic seizures associated with focal cortical dysplasia type II - FCDS-02

Kato Mitsuhiro0 个研究点目标入组 15 人开始时间: 2019年12月11日最近更新:

试验速览

阶段
2 期
状态
进行中(未招募)
发起方
入组人数
15

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
>= 2age old 至 ot applicable(—)
性别
All

入选标准

  • 1.After completion of clinical trial (FCDS-01 or Hokudai FCDS or sirolimus Shizuoka 2019-1), age >= 2 years old; bodyweight >= 10kg
  • 2.Improvement of epileptic seizures by FCDS-01 or Hokudai FCDS or sirolimus Shizuoka 2019-1
  • 3.No severe adverse effect by sirolimus or antiepileptic drugs in preceding clinical trial (FCDS-01 or Hokudai FCDS or sirolimus Shizuoka 2019-1)
  • 4.Informed consent by written agreement after precise explanation

排除标准

  • 1.Patients without accurate data of compliance, adverse event, seizure frequency, duration of seizure
  • 2.Possible attendance another clinical trial
  • 3.Prescription of PB or VGB
  • 4.Possible ketogenic diet therapy
  • 5.Pregnant patient or no agreement for contraception
  • 6.Basic disease inflammation, degenerative diseases
  • 7.Risk of suicide
  • 8.History of alcoholic abuse
  • 9.Among preceding clinical trial (FCDS-01 or Hokudai FCDS or sirolimus Shizuoka 2019-1), the following laboratory data were observed
  • 9-1 AST or ALT >= 2.5 folds of standard value in our hospital
  • 9-2 WBC < 3000 /mm3, Ht < 30%, Platelet < 80000/mm3, neutrophils < 1000/mm3
  • 9-3 C cr < 50ml/min, eGFR < 30mL/min/1.73m2
  • 9-4 HBsAg (+), HBs Ab(+) after HBV infection, HBc Ab (+)
  • 9-5 Uncontrolled hyperlipidemia
  • 10.Association of arrythmia or cardiac failure requiring treatment.
  • 11.Association of immunodeficiency
  • 12.Irregular visit to hospital
  • 13.Decision of inappropriate patient for this study by responsible doctor

研究者

发起方
Kato Mitsuhiro

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Research of sirolimus administration for FCD II type | 临床试验