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The effect of Turmeric on blood Indicators and blood pressure in hyperlipidemic type 2 diabetes mellitus patients

The effect of Turmeric on blood Indicators and blood pressure in hyperlipidemic type 2 diabetes mellitus patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201204162602N7
Enrollment
80
Registered
2012-05-12
Start date
2012-06-20
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

hyperlipidemic type 2 diabetes mellitus patients. Diabetes mellitus

Interventions

Intervention 1: group receiving turmeric:capsules containing 800mg turmeric, three a day for 8 weeks. Intervention 2: placebo group receiving :capsules containing 800mg of corn starch, three a day for
Treatment - Drugs
Placebo
group receiving turmeric:capsules containing 800mg turmeric, three a day for 8 weeks
placebo group receiving :capsules containing 800mg of corn starch, three a day for 8 weeks

Sponsors

Tehran university of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Willingness to participate in the study; People with type 2 diabetes; Aged people with 30 to 70 years of age; Aged people with 30 to 70 years of age; People having HbA1c above 6; Patients with TG>150mg/dl, LDL above 100mg/dl; Lack of consumption of multivitamin; supplements, antioxidants, polyphenols, since last three months; BMI 20 – 35 . Exclusion criteria of the study: Participants of the study under treatment had no changes in consumption of medicine; Patients having fasting blood glucose >200mg/dl or LDL>160mg/dl were excluded from the study; Changes in dose and type of medication; Inclusion criteria for the study: Acute cardiac disease, renal failure, liver and thyroid disease; Rejection of turmeric powder supplement. actation or pregnancy; Severe gastrointestinal disease and gastric ulcers; Risk of gall stones Changes in physical activity and diet;

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Systolic blood pressure. Timepoint: 8 weeks. Method of measurement: sphygmomanometer.;Diastolic blood pressure. Timepoint: 8 weeks. Method of measurement: sphygmomanometer.;FBS. Timepoint: 8 week. Method of measurement: Laboratory kit.;Fasting Insulin. Timepoint: 8 week. Method of measurement: Laboratory kit.;HbA1C. Timepoint: 8 weeks. Method of measurement: Laboratory kit.;Triglyceride (TG). Timepoint: 8 weeks. Method of measurement: Laboratory kit.;Total Cholesterol (TC). Timepoint: 8 weeks. Method of measurement: Laboratory kit.;LDL. Timepoint: 8 weeks. Method of measurement: Laboratory Kit.;HDL. Timepoint: 8 weeks. Method of measurement: Laboratory Kit.;Apo A-I. Timepoint: 8 weeks. Method of measurement: Laboratory Kit.;Apo B-100. Timepoint: 8 weeks. Method of measurement: Laboratory kit.;CRP. Timepoint: 8 weeks. Method of measurement: Laboratory kit.;TAC. Timepoint: 8 weeks. Method of measurement: Laboratory kit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohreh Adab

school of health tehran university of medicalSciences

Zohre_adab2000@yahoo.com+98 21 8877 9118

Outcome results

None listed

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