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Investigation of the effects of curcuminoids on the risk of heart disease

Investigation of the effects of supplementation with curcuminoids on on cardiovascular risk factors in obese dyslipidemic subjects

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013082914521N1
Enrollment
30
Registered
2013-09-14
Start date
2010-08-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: Dyslipidemia. Condition 2: Obesity.

Interventions

Intervention 1: Curcuminoids are bioactive ingredients of turmeric. They belong to the polyphenol group of phytochemicals. The chemical name of curcumin is (1E,6E)-1,7-Bis(4-hydroxy-3-methoxyphenyl)-1
Treatment - Drugs
Placebo
Curcuminoids are bioactive ingredients of turmeric. They belong to the polyphenol group of phytochemicals. The chemical name of curcumin is (1E,6E)-1,7-Bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,
Control group: placebo for 4 weeks

Sponsors

Mashhad University of Medical Sciences Research Council
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: obese subjects (with body mass index (BMI) = 30) who had either < 2 risk factors (except diabetes mellitus) for coronary heart disease (CHD) plus 160 mg/dL < LDL-C < 190 mg/dL, or = 2 CHD risk factors (except diabetes mellitus) and 130 mg/dL < LDL-C < 160 mg/dL. Exclusion criteria were history of systemic diseases (such as systemic lupus erythematosus, kidney disease, diabetes mellitus and established cardiovascular disease), consumption of drug supplements within the preceding 6 months and history of taking any lipid-lowering drug. Exclusion criteria: systemic disease or history of systemic disease (such as lupus, kidney disease, diabetes mellitus); history of cardiovascular disease; BMI < 30; consumption of drug supplements within the 6 months and history of taking any lipid lowering drug.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Total cholesterol. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Routine enzymatic methods using standard biochemistry kits on an autonalyzer.;Triglycerides. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Routine enzymatic methods using standard biochemistry kits on an autonalyzer.;HDL cholesterol. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Routine enzymatic methods using standard biochemistry kits on an autonalyzer.;LDL cholesterol. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Routine enzymatic methods using standard biochemistry kits on an autonalyzer.

Secondary

MeasureTime frame
Vitamins. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Enzymatic assay.;Lipoprotein(a). Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Enzyme immunoassay.;Cathepsin D. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Enzyme immunoassay.;Vitamin C, vitamin E, lipoprotein(a) and cathepsin D. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Questionnaire, enzymatic and immunoassay kits.;Anxiety. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Questionnaire.;Serum small dense LDL. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Enzyme immunoassay.;Heat shock protein 27 antibodies. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Enzyme immunoassay.;Pro-oxidan-antioxidant blance. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Colorimetric assay.;Cytokines. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Enzyme immunoassay.;Superoxide dismutase. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Enzymatic assay.;Zinc. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Enzymatic assay.;Copper. Timepoint: Baseline, week 4, week 6 and week 10. Method of measurement: Enzymatic assay.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMajid Ghayour-Mobarhan

Cardiovascular Research Center, Mashhad University of Medical Sciences

ghayourm@mums.ac.ir+98 51 1882 9260

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026