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临床试验/JPRN-jRCT2091220231
JPRN-jRCT2091220231已完成2 期

Multicenter cooperative and investigator initiated clinical trial using valproic acid in childhood onset spinal muscular atrophy : Confirmatory Trial - SMART02

Institute of Medical Genetics, Tokyo Women's Medical University0 个研究点目标入组 28 人开始时间: 2015年12月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
28

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
>= 1age old 至 < 7age old(—)
性别
All

入选标准

  • (1) Patients with SMN 1 gene mutation proven by gene testing
  • (2) Patients of SMA types 1 and 2.
  • (3) Patients with stable head and neck
  • (4) HFMSE score > 1point
  • (5) Patients who can visit the hospital as scheduled in clinical trials.
  • (6) Patients with a guardian under conditions below
  • 1) A fixed guardian can comprehend the status of the patient and observe the patient's daily activities as required in the clinical trial.
  • 2) Management of medicine is definitely possible.

排除标准

  • (1)Patients who have had an operation for spinal scoliosis.
  • (2)Patients on mechanical ventilator with tracheotomy or who are judged to require mechanical ventilation with tracheotomy by the investigator (or sub-investigator).
  • (3)Patient with severe liver dysfunction, renal dysfunction, and circulatory diseases. (judged referring to grade 3 of Severity Criteria for Drug Adverse Reaction Yaku-Ann No 80, issued by the chief of Registration Division the Pharmaceutical Affairs Bureau, Ministry of Welfare)
  • (4)Patients given Riluzole, creatine, butyric acid compound, steroid hormone and sodium valproate within 8 weeks before the agreement was obtained.
  • (5)Patients with malignant tumors
  • (6)Patients with severe medical history of drug allergy such as anaphylactic shock, or serious side effect of drug.
  • (7)Patients participating in other clinical trials and administered an investigational new drug within 12 weeks before obtaining the agreement for this clinical trial.
  • (8) Patients scheduled to take a carbapenem antibiotic within the period from agreement to the end of observation.
  • (9) Patients who have started physical therapy for less than four weeks before obtaining the agreement for this clinical trial. Starting the respiratory physical therapy is accepted.
  • (10) Patients with urea cycle abnormalities.
  • (11) Other patients judged to be unsuitable to join this clinical trial by the investigator (or sub-investigator).

研究者

发起方
Institute of Medical Genetics, Tokyo Women's Medical University

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