A Randomized, Double-Blind, Three-Arm, Placebo-Controlled, Comparative, Clinical Study to Evaluate the Efficacy of Nutraceutical Test Samples (As coded Test Products A, B and C) on Healthy Adult Subjects.

Patanjali Ayurved Ltd0 个研究点目标入组 52 人开始时间: 待定最近更新: 2024年6月24日

试验速览

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•1.Age: 35 to 50 years (inclusive) at the time of consent.
•2.Sex: Males and Non-pregnant/Non-lactating Females (preferably equal numbers of males and females).
•3.Females of Childbearing potential must have a negative urine pregnancy test performed on screening visit and agree to follow an accepted method of birth control for the duration of the study.
•4.Corporate Subjects with complaint of feeling exhausted with routine and impaired due to lack of energy.
•5.Subjects with ability to understand and willingness to sign and date a written Informed Consent Document at the screening visit before any protocol- specific procedures are performed.
•6.Subjects willing to follow all study instructions and report to facility for all follow-up visits.

•1.Subjects with acute and chronic diseases (including diabetes, inflammatory bowel diseases, dementia, multiple sclerosis).
•2.History of substance or alcohol abuse within the last 2 years.
•3.Subjects who are using additional suppliments, using medications (e.g. antihypertensive medications, lipid reducers, thyroid medication).
•4.Female subjects who are Pregnant or lactating women.
•5.Any individual who is involved with conduct of this study.
•6.Subjects who have participated in another study with any investigational product within 3 months of randomization.
•7.Subject having history of/or currently using medication which in the opinion of the investigator may affect the evaluation of the study product, or place the participant at undue risk.
•8.Any disease or condition that in the opinion of the investigator and/or sponsor may interfere with the completion of the study evaluation.

发起方

Patanjali Ayurved Ltd