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Effect of curcumin (tumeric) on patients with Metabolic syndrome

Clinical trial of curcumin effect on patients with Metabolic syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201512181165N12
Enrollment
100
Registered
2017-10-27
Start date
2015-12-22
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

Metabolic Syndrome. Other postprocedural endocrine and metabolic disorder

Interventions

Intervention 1: Intervention group: Curcumin capsule, once a day for 3 months. Intervention 2: Control group: Placebo of curcumin, once a day for 3 months.
Treatment - Drugs
Placebo
Intervention group: Curcumin capsule, once a day for 3 months
Control group: Placebo of curcumin, once a day for 3 months

Sponsors

Baghiyatallah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Patients with metabolic syndrome; Sign informed consent Exclusion Criteria: Discontinue of treatment for more than One week; Allergic reaction to herbal compounds; Abnormal results in lab tests

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Blood Pressure. Timepoint: Before and after of intervention (12 weeks). Method of measurement: mmHg.;FBS. Timepoint: Before and after of intervention (12 weeks). Method of measurement: mg/dl.;TG. Timepoint: Before and after of intervention (12 weeks). Method of measurement: mg/dl.;HDL. Timepoint: Before and after of intervention (12 weeks). Method of measurement: mg/dl.;LDL. Timepoint: Before and after of intervention (12 weeks). Method of measurement: mg/dl.;Small Density LDL. Timepoint: Before and after of intervention (12 weeks). Method of measurement: mg/dl.;Interleukin 8. Timepoint: Before and after of intervention (12 weeks). Method of measurement: Level of serum.;Interleukin 6. Timepoint: Before and after of intervention (12 weeks). Method of measurement: Level of serum.;Hb A1C. Timepoint: Before and after of intervention (12 weeks). Method of measurement: Level of serum.;Leptin. Timepoint: Before and after of intervention (12 weeks). Method of measurement: ng/ml.;Adiponectin. Timepoint: Before and after of intervention (12 weeks). Method of measurement: ng/ml.;Leptin/Adiponectin Ratio. Timepoint: Before and after of intervention (12 weeks). Method of measurement: Ratio.

Secondary

MeasureTime frame
Body Mass Index (BMI). Timepoint: Before and after of intervention (12 weeks). Method of measurement: Kg/m2.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNiloufar Torabi

Pharmaceutical Sciences Branch Islamic Azad University

y_niloo@yahoo.com+98 21 2264 0051

Outcome results

None listed

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