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nanomicielles curcumin in metabolic syndrome

Study of the effect of nanomicelles curcumin on glycemic control, serum lipid profile ,blood pressure and anthropometric measurements in patients with metabolic syndrome

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150815023617N3
Enrollment
21
Registered
2018-06-25
Start date
2018-05-30
Completion date
Unknown
Last updated
2018-07-16

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

Conditions

Metabolic syndrom. Metabolic syndrome

Interventions

Intervention 1: Intervention group: Each capsule contains 80 mg nanomicielles curcumin. Use once a day for 12 weeks. Intervention 2: Control group: Each capsule contains yellow colour(E104) and lecit

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Tendency for participation Age between 18-70 years old BMI between 25-40 kg/m2 Having metabolic syndrome according to the NCEP ATP III definition(if patient have three or more of the following five criteria): waist circumference over 120 cm (men) or 89 cm (women), blood pressure over 130/85 mmHg, fasting triglyceride (TG) level over 150 mg/dl, fasting high-density lipoprotein (HDL) cholesterol level less than 40 mg/dl (men) or 50 mg/dl (women) and fasting blood sugar over 100 mg/dl.

Exclusion criteria

Exclusion criteria: Pregnancy Lactation Use insulin injection Thyroid disorder Henal disease Having unusual diet during 3 last month Use weight loss and fat burner drugs

Design outcomes

Primary

MeasureTime frame
Homeostatic model assessment of insulin resistance(HOMA-IR). Timepoint: Baseline and end of the study. Method of measurement: Calculation :(glucose×Insulin)/22.5.;Homeostatic model assessment of B-cell function(HOMA-B). Timepoint: Baseline and end of the study. Method of measurement: Calculation.;Hba1c. Timepoint: Baseline and end of the study. Method of measurement: ion-exchange chromatography.;Serum glucose. Timepoint: Baseline and end of the study. Method of measurement: Colorimetric analysis method.;Serum insulin. Timepoint: Baseline and end of the study. Method of measurement: ELISA method.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohre Bateni

Shahid Beheshti University of Medical Sciences

zohre.bateni@yahoo.com+98 21 2236 0656

Outcome results

None listed

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