A randomized placebo controlled trial of Ayush SR in Perceived stress

Central council for research in Ayurvedic Sciences Ministry of Ayush Government of India0 个研究点目标入组 0 人开始时间: 待定最近更新: 2022年10月17日

试验速览

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•I.Participants with concurrent serious Hepatic Dysfunction (defined as AST and/or ALT > 2 times of the upper normal limit) or Renal Dysfunction (defined as S. creatinine > 1.2 mg/dl)
•II.History of cardiovascular, pulmonary, neurological, endocrine diseases or other concurrent severe disease.
•III.Lifetime history of psychotic disorders of any type, bipolar disorder, schizophrenia or schizoaffective disorder and other psychiatric disorders such as other anxiety disorders, major depressive disorder,
•IV.A diagnosis of any organic brain disease, mental retardation, or other cognitive dysfunction that could interfere with their capacity to participate in the study
•V.Participants on any psychotropic medications, mood stabilizers or benzodiazepines
•VI.History of alcohol or drug dependence.
•VII.History of uncontrolled diabetes (HbA1c > 8 %), Uncontrolled Hypertension (Resting blood pressure Ã¢â?°Â¥ 160 systolic and/or 100 diastolic)
•VIII.Participants with uncontrolled Hypothyroidism/ hyperthyroidism even with medication.
•IX.Participants with sub-clinical hypothyroidism (TSH 4.5 to 10 mIU/L) which require active therapy
•X.Pregnant / lactating women.
•XI.Participants who have completed participation in any other clinical trial during the past 3 months.
•XII.Any other condition which the investigator thinks may jeopardize the study.

发起方

Central council for research in Ayurvedic Sciences Ministry of Ayush Government of India