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临床试验/CTRI/2023/09/057859
CTRI/2023/09/057859尚未招募1 期

Clinical validation of safety and efficacy of herbal blends to alleviate stress and anxiety along with improved mood status in healthy individuals. - Nil

Sush Essentials Pvt. Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
1 期
状态
尚未招募
发起方

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 meeting all of the following criteria will be eligible for the study:
  • 1.Healthy male or female 25-55 years of age at the time of obtaining written informed consent
  • 2.Subjects willing to sign inform consent form
  • 3.A female participant who is of reproductive potential has a negative pregnancy test and agrees to use contraception throughout the study period
  • 4.Subjects are free of anti-depressants /anti-anxiety/ mood enhancing/recreational drugs intake for at least one year at the start of the screening visit
  • 5.Subjects are free of any ‘‘over the counter’’ or prescribed medications at the start of the screening visit
  • 6.Subjects with a score of 7-26 on the Perceived Stress Scale (PSS)
  • 7.Willing to abstain alcohol, caffeine, and nicotine consumption while in the study
  • 8.No reported history of psychological or mental disorders.
  • 9.Free of psychiatric conditions other than perceived stress

排除标准

  • Subjects meeting any of the following criteria will not be eligible for the study:
  • 1.Resting systolic blood pressure above 140 mmHg or a diastolic blood pressure above 90 mmHg at baseline visit.
  • 2.Taking any medicine or dietary supplements within the last 3 months to help to relieve sleep disturbances or physiological stress
  • 3.History of substance abuse or dependence
  • 4.Taking certain prohibited medications
  • 5.Habitual smoking or vaping of products nicotine containing tetrahydrocannabinol (THC) with an average consumption >2 cigarettes or vaping more than 2 times per day
  • 6.History of malignancy less than or equal to 5 years prior to signing an informed consent
  • 7.Other conditions, which in the opinion of the investigators, makes the subject unsuitable for enrolment or could interfere with his/her participation in, and completion of the protocol.
  • 8.Any known allergy or intolerance to any of the ingredients contained in supplements

研究者

发起方
Sush Essentials Pvt. Ltd

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