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临床试验/CTRI/2020/08/027076
CTRI/2020/08/027076已完成2 期

A Prospective, parallel arm randomized clinical study to evaluate safety and efficacy of HFSM-02 in reducing stress and anxiety in subjects with chronic medical condition and perceived stress - NI

Siddhayu Ayurvedic Research Fdn Pvt Ltd0 个研究点目标入组 120 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
120

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

  • Subjects of age between 18 and 60 years
  • Free of psychiatric conditions other than stress
  • Have a score less than 15 on the World Health Organizationâ??five (WHO-5) well-being index and a score of at least 14 on the Perceived Stress Scale (PSS)
  • CHD patients showing one or more of the following conditions like hypertension, dyslipidemia, atherosclerotic, ischemic changes, with certain psychological stress-related complaints mainly irritation, anxiety, etc. on stable medical prescriptions.
  • Prediagnosed diabetes type 2 patients with HbA1c including but NMT 7.5 with certain psychological stress-related complaints mainly irritation, anxiety, etc. and on stable medical prescription

排除标准

  • Subjects suffering from any chronic physical, neurological or psychiatric illness
  • Subjects currently undergoing active MI episode
  • Subjects with uncontrolled diabetes
  • Subjects with compromised liver or renal function test as per sole discretion of investigator that can prove the subject unfit for the trial
  • Subjects currently taking any herbal preparations or formulations containing Ashwagandha, ginseng, ginkgo biloba, Brahmi or related herbs,
  • Subjects pregnant or lactating
  • Subjects with substance dependence
  • Subjects in investigators opinion not fit for the study.

研究者

发起方
Siddhayu Ayurvedic Research Fdn Pvt Ltd

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