跳至主要内容
临床试验/CTRI/2023/01/049316
CTRI/2023/01/049316已完成2 期

A double blind, randomized, placebo controlled Clinical Study to Evaluate the efficacy of Menoveda Akira tablet in patients having menopause related mental health issues.

Menoveda Lifesciences Pvt Ltd0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
60

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

入选标准

  • 1.Females from 45 to 70 years of age, post Menopause.
  • 2.Females suffering from one or multiple mental health issues from- anxiety, insomnia, depression etc;
  • 3.Females that are able to give written informed consent in a manner approved by the institutional ethics committee and comply with the requirements of the study.
  • 4.Females willing to avoid participation in any other interventional clinical trial for the duration of the study.

排除标准

  • 1.Have used, are using, or are planning to use immunosuppressive or immunomodulatory medication (i.e., biologics), including oral or parenteral corticosteroids.
  • 2.Females that have participated in any other interventional clinical trial in the previous 30 days.
  • 3.Females with known sensitivity to any of the constituents of the investigational product.

研究者

发起方
Menoveda Lifesciences Pvt Ltd

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