CTRI/2021/04/033039Not yet recruitingPhase 2
A comparative clinical study to assess the effect ofSanshodhanKarma i.e. Vaman and Virechan on lipid profile.
Trial Snapshot
- Phase
- Phase 2
- Status
- Not yet recruiting
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •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
Exclusion Criteria
- •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.
Investigators
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