Skip to content

Comparative Study of Efficacy and Adverse Effects of Triphala versus Simvastatin in Blood Lipids Reduction in Dyslipidemia Patients.

Comparative Study of Efficacy and Adverse Effects of Triphala versus Simvastatin in Blood Lipids Reduction in Dyslipidemia Patients. (Clinical Trial Phase II)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20140523002
Enrollment
Unknown
Registered
2014-05-23
Start date
2014-05-26
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dyslipidemia Dyslipidemia Triphala Simvastatin

Interventions

Triphala powder capsule at dose of 500 mg two times a day after meal (morning and evening) daily for 90 days,Placebo capsule at dose of 500 mg one times a day after morning meal daily for 90 days Simv
Experimental Drug,Experimental Drug
Triphala,Simvastatin

Sponsors

Department for Development of Thai Trditional and Alternative Medicine
Lead Sponsor
Faculty of Medicine&#44
Collaborator
Thammasat University
Collaborator

Eligibility

Sex/Gender
All
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1 Body Mass Index 18 to 35 kilometer per square meter 2 Total Cholesterol 200 to 300 milligram per deciliter and Low Density Lipoprotein cholesterol 130 to 189 milligram per deciliter 3 have at least 2 risk factors listed below Cigarette smoking Hypertension Blood pressure more than 140 over 90 milimeter of mercury or on antihypertensive medication Low High Density Lipoprotein cholesterol Family history of premature chronic heart disease CHD in male first degree relative Age men more than 45 years women more than 55 years 4 Volunteer have a normal Complete Blood Count laboratory and liver function tests 5 volunteer are currently use medicine for lipid reduction They must stop the drug for a period of 30 days before the start of medication project in order to get rid of fat levels of drugs from body and blood

Exclusion criteria

Exclusion criteria: 1 Dyslipidemia with secondary type is caused by one or more of the following diseases nephrotic syndrome cholestasis hypothyroidism 2 who eat other herbal medicines or supplements that affect blood fat levels such as steroid tegretol cyclosporine fish oil cholesterol absorption inhibitor fibrate Niacin acid binding Bile resins Statins probucol thiazides beta blockers testosterone estrogen progestogens glucocorticoids etc that can t stop the drug 3 Who is participating in other research projects 4 History of allergy or Simvastatin or allergy herbal medicine 5 had high risk factors for heart diseases and blood diseases such as cardiovascular leaders and those who have other diseases that have a risk of coronary artery disease are equivalent type II diabetes ischemic stroke which is caused by atherosclerosis carotid artery carotid artery transient ischemic attack Symptomatic disease peripheral arterial disease abdominal aortic aneurysm and those with vascular complications 6 Liver cancer or complications of liver and kidney dysfunction is Glomerular filtration rate less than 60 mililiter per min 7 Pregnant or nursing child

Design outcomes

Primary

MeasureTime frame
efficacy 2 year blood test

Secondary

MeasureTime frame
Adverse Effects 2 year Questionaire

Countries

Thailand

Contacts

Public ContactPeerapong Kittipawong

Faculty of Medicine, Thammasat University

p.kittipawpng@gmail.com081-6441649

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026