Health Condition 1: E785- Hyperlipidemia, unspecified
Conditions
Interventions
None listed
Sponsors
Dr. Neha Rani
Eligibility
Inclusion criteria
Inclusion criteria: Patients aged 21-60 years and having the level of bad lipids above the upper limit of normal range but below the lower level of the range mentioned as high value by WHO. Patient currently not taking lipid lowering medication such as statin, fibrates, niacin since the last 4 weeks. Patient who has given written informed consent to participate in trial and agreement to abstain from any new supplement or herbal preparation during the study.
Exclusion criteria
Exclusion criteria: If patient is having any grave health problem like liver cirrhosis, Renal insufficiency Cardiovascular events such as MI, stroke cardiac surgery within last 6 months. Pregnant women, lactating women or those planning conception during the study period. If patient is on medications affecting the lipid metabolism like corticosteroids, beta blocker and oral contraceptives.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The trial drugs selected for the study viz. churna kalpana of root bark and stem bark of kanchnar is effective in management of dyslipidemia. Any of those two can be more effective.Timepoint: The duration of intervention will be 60 days.Follow up of the patient will be done after 30 days and 60 days after enrollment of patient in study.The assessment of objective criteria that are lab investigations will be done on ist day of study that is before starting of medication, after 30 days of medication and after 60 days of medication. | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Public ContactDr Naresh Kumar
MSM Institute of Ayurveda, BPSMV, Khanpur Kalan, Sonipat, 131305, Haryana
Outcome results
None listed