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临床试验/NCT01203592
NCT01203592已完成1 期

Efficacy of Albuterol in the Treatment of Congenital Myasthenic Syndromes

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2010年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
Mayo Clinic
入组人数
21
试验地点
1
主要终点
Name: Efficacy of albuterol in the treatment of congenital myasthenic syndromes

研究概览

简要总结

The study tests the notion that patients suffering from certain types of congenital myasthenic syndromes are benefitted by the use of Albuterol at doses used in clinical practice.

详细描述

The aim of the proposal is to evaluate the effects of albuterol, an adrenergic agonist, in the treatment of congenital myasthenic syndromes (CMS). Over the past 2 decades I found that some CMS patients refractory to or worsened by cholinergic agonists, namely those suffering from defects in acetylcholinesterase (AChE) or Dok-7, respond to ephedrine, a medication used for over half-a-century in the treatment of autoimmune myasthenia gravis. After ephedrine became unavailable, I treated the same type of patients with albuterol in doses ranging from 4 mg daily to twice daily for adults; the dose for children 6 to 12 years is 2 mg two or three times daily; the dose for children 2 to 6 years is 0.1 mg/kg/day (maximum 2 mg) three times daily. Evaluation of the effects of the medications are based on the Table shown below.

Name:

Mayo Clinic no:

Date of this report: (dd/mm/yyyy):

Before taking Albuterol ER On Albuterol (date of this report)

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
2 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of congenital myasthenic syndrome substantiated by typical clinical history, seronegativity to AChR and MuSK, and evidence of a decremental EMG response.

排除标准

  • Uncontrolled hypertension, arrhythmias, or other significant cardiac disease.

研究组 & 干预措施

Albuterol

Experimental

4 mg twice daily by mouth for adults. The dose for children 6 to 12 years is 2 mg two or three times daily; the dose for children 2 to 6 years is 0.1 mg/kg/day (maximum 2 mg) three times daily.

干预措施: Albuterol (Drug)

结局指标

主要结局

Name: Efficacy of albuterol in the treatment of congenital myasthenic syndromes

时间窗: 3 years

The primary outcome measures pertain to evaluating the improvement in the patient's strength

次要结局

未报告次要终点

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Andrew Engel

PI

Mayo Clinic

研究点 (1)

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