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临床试验/IRCT138803061965N1
IRCT138803061965N1已完成未知

Prospective Evaluation of the Midodrine Efficacy in the Treatment of Vasovagal Syncope: A Randomized Placebo-Controlled Study

Research department of Rajaie Cardiovascular Medical and Research Center0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
100

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
15 years 至 80 years(—)
性别
All

入选标准

  • (1) a frequency of at least one episode of syncope during previous 6-month and (2) a positive head-up tilt test.
  • Exclusion criteria: (1) other causes of syncope; (2) cardiovascular
  • and /or systemic disease; or (3) systolic blood pressure >150 mmHg or diastolic blood pressure >95 mmHg; or (4) thyrotoxicosis; or (5) renal failure; or (6) pheochromocytoma.

排除标准

  • 未提供

研究者

发起方
Research department of Rajaie Cardiovascular Medical and Research Center

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Midodrine Versus Placebo in VasoVagal Syncope | 临床试验