CTRI/2024/05/066815尚未招募4 期
A Randomized, Placebo-controlled Clinical Study to Evaluate the Efficacy and Safety of Meet Shilajeet Supplement on Improving Vitality, Boosting stamina, Strength and Performance in Healthy Adults. - NI
Herbal Creations0 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
- 4 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
- •1) Healthy male adult subjects age between 18–45 years.
- •2) Participants with a body mass index (BMI) of 18.5–29.9 kg/m2
- •3) Willing to participate in an exercise program 2-3 times per week for 8 weeks.
- •4) Subjects should be available for duration of study period (8 weeks).
- •5) Express a willingness to actively participate in the study and provide informed consent.
排除标准
- •1) Individuals currently undertaking resistance training exercise.
- •2) Clinically significant medical conditions, including but not limited to cardiovascular, neurological, psychiatric, renal, immunological, endocrine (such as uncontrolled diabetes or
- •thyroid disease), or haematological abnormalities.
- •3) Taking medication with corticosteroids, antidepressants, anticholinergics, or any other drugs that may have influenced the study outcome.
- •4) Severe pulmonary dysfunction (uncontrolled bronchial asthma and/or chronic obstruction).
- •5) History of orthopaedic conditions or surgeries that would interfere with exercise performance.
- •6) Completed any other clinical trial within 6 months prior to enrolment.
- •7) Consumed any dietary supplements or herbal drugs within 7 days prior to screening.
- •8) Known hypersensitivity to herbal drugs, nutritional supplements, or foods.
- •9) Active smokers or having a history of high alcohol intake (2 standard drinks per day)
研究者
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