CTRI/2019/12/022521已完成未知
Homoeopathic drug proving: Randomized double-blind placebo-controlled trial of PRO1 - Nil
ife Force Foundation Trust0 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
- 未知
- 状态
- 已完成
- 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 individuals with no apparent disease and normal routine laboratory parameters during screening
- •2.Intelligent enough to record carefully the facts, subjective and objective symptoms generated by the drug during proving.
- •3.Able to be informed of the nature of the study and willing to give written informed consent
排除标准
- •1.Any disease or condition which might compromise the hematopoietic, renal, endocrine, pulmonary, central nervous system, cardiovascular, immunological, dermatological, gastro-intestinal or any other body system
- •2.Persons with colour blindness.
- •3.Persons who have undergone surgery in last two months.
- •4.Planned medical / dental treatment during the proving period including herbal or dietary supplements, procedures, or medications that are likely to interfere with, or substantially alter, responsiveness to the proving substance.
- •5.Volunteers on regular medication (allopathic, ayurvedic, homoeopathic, naturopathic, unani, etc.) for any acute or chronic disease.
- •6.Participant must not be on any homoeopathic remedy in the preceding one month and have had no significant change in health status in last one month.
- •7.Emotionally disturbed, hysterical or anxious persons.
- •8.Persons having known history of allergies, food hypersensitivity, etc.
- •9.Women during pregnancy, puerperium and while breast-feeding.
- •10.Smokers who smoke more than 10 cigarettes per day
- •11.Recent history of alcoholism / drug addictions or unlikely to refrain from excessive alcohol consumption / drug intake during the study period
- •12.Participation in another clinical or proving trial during the last 6 months
研究者
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