跳至主要内容
临床试验/CTRI/2021/04/033039
CTRI/2021/04/033039尚未招募2 期

A comparative clinical study to assess the effect ofSanshodhanKarma i.e. Vaman and Virechan on lipid profile.

ational Institute of Ayurveda0 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
2 期
状态
尚未招募

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. Male or Female Subjects in the age group of 18 to 60 years, both inclusive.
  • 2. Subjects who are willing to undergo sanshodhan karma.
  • 3. Subjects of female gender or non-pregnant, non-lactating females. A urine pregnancy test
  • is required for all female subjects of childbearing potential unless subject has had a
  • hysterectomy, tubal ligation, or is > 2 years postmenopausal.
  • 4. Subjects willing to follow the procedures as per the study protocol and voluntarily sign an
  • informed consent form

排除标准

  • 1. Subjects with any known systemic disease.
  • 2. Known cases of Severe/Chronic hepatic or renal disease.
  • 3. Known case of any active malignancy.
  • 4. Subjects giving history of significant cardiovascular event.
  • 5. Subjects having known chronic, contagious infectious disease, such as active
  • tuberculosis, Hepatitis B or C, or HIV.
  • 6. Pregnant and Lactating females.
  • 7. Those who are contraindicated for sanshodhan karma.

研究者

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