CTRI/2025/04/084358Not yet recruitingPhase 4
A comparative clinical study to evaluate the effect of Shadushan Guggulu and Triphala kwath in the management of Medoroga w.s.r. to Dyslipidemia
Prof Dr Vijay Chaudhary1 site in 1 country30 target enrollmentStarted: June 20, 2025Last updated:
Trial Snapshot
- Phase
- Phase 4
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- To reduce the level of S.Cholesterol level below 200mg/dl
Study Overview
Brief Summary
At the end of the trial, collected data will be analyzed by using appropriate statistical methods and will be present in the form of thesis.
Study Design
- Study Type
- Interventional
- Allocation
- Not Applicable
- Masking
- Not Applicable
Eligibility Criteria
- Ages
- 30.00 Year(s) to 70.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patients with Serum lipid profile : Serum Cholesterol- 200 to 350 mg/dl Serum Triglycerides.
- •150 to 350 mg/dl Serum LDL.
- •100 to 200 mg/dl Serum VLDL.
- •30 to 100 mg/dl Serum HDL.
- •20 to 40 mg/dl Patients willing to participate in the trial. Patients between the age group of 30-70 years of either gender will be selected for the study.
Exclusion Criteria
- •Patient having major illness like Type-II Diabetes mellitus, Carcinoma, advanced Renal and Liver disorders.
- •Pregnant females and lactating mother.
- •Patients who has completed participation in any other clinical trial during the past 6 months.
Outcomes
Primary Outcomes
To reduce the level of S.Cholesterol level below 200mg/dl
Time Frame: 3 months
S.Triglycerides level below 150mg/dl
Time Frame: 3 months
S.LDL level below 100mg/dl
Time Frame: 3 months
Secondary Outcomes
- To assess the clinical safety of Shadushan Guggulu and Triphala Kwath in patients of Medoroga w.s.r. to Dyslipidaemia.(3 months)
Investigators
Study Sites (1)
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