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临床试验/IRCT20181208041882N16
IRCT20181208041882N16已完成3 期

Comparison of the effectiveness of Vitagnos, Gabapentin and Paroxetine on the early complications of menopause in women: a double-blind clinical trial.

Yazd University of Medical Sciences0 个研究点目标入组 90 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
90

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
45 years 至 60 years(—)
性别
Female

入选标准

  • Age 45 to 60 years
  • Amenorrhea for at least 12 months
  • At least 3 hot flushes in 24 hours

排除标准

  • Women with abnormal menopause
  • Patients with chronic diseases (thyroid disease, psychosomatic disease, pheochromocytoma, carcinoid, leukemia, cancer and other known systemic diseases such as hypertension, diabetes, heart diseases)
  • Consumption of hormones and supplements (containing estrogen-like compounds such as soy)

研究者

发起方
Yazd University of Medical Sciences

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