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The effect of Ellagic acid supplementation in patients with type 2 diabetes

The effect of ellagic acid supplementation on glycemic indices, lipid profile, anthropometric, inflammatory and oxidative indices, dietary intake and serum levels of pentosidine, adiponectin and resistin in patients with types 2: a double-blind, randomized controlled clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20121028011288N18
Enrollment
46
Registered
2022-10-26
Start date
2022-10-21
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

type 2 diabetes. Type 2 diabetes mellitus

Interventions

Intervention 1: Intervention group: Patients in this group will receive 1capsules of 250 milligrams of ellagic acid (product by Exir Gostar Espadana Co. and made in The Iran) for 8 consecutive weeks a

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: patients with type 2 diabetes Using blood sugar lowering medicine Age range of 30-60 years BMI in the range of 25-35 1 to 15 years duration of type 2 diabetes Tendecy of corporation

Exclusion criteria

Exclusion criteria: Use of corticosteroids, steroidal and non-steroidal anti-inflammatory drugs Prescribing insulin Suffering from chronic diseases such as heart failure, kidney, liver and thyroid disorders

Design outcomes

Primary

MeasureTime frame
Serum level of pentosidine. Timepoint: At the beginning of the study and 60 days later. Method of measurement: ELISA kit.;Serum level of adiponectin. Timepoint: At the beginning of the study and 60 days later. Method of measurement: ELISA kit.;Serum level of resistine. Timepoint: At the beginning of the study and 60 days later. Method of measurement: ELISA kit.;Fasting blood sugar. Timepoint: The beginning of the study and 60 days later. Method of measurement: Enzymatic kit.;Total cholesterol. Timepoint: The beginning of the study and 60 days later. Method of measurement: Enzymatic kit.;Serum triglyceride. Timepoint: The beginning of the study and 60 days later. Method of measurement: Enzymatic kit.;HDL serum level. Timepoint: The beginning of the study and 60 days later. Method of measurement: Enzymatic kit.;LDL serum level. Timepoint: The beginning of the study and 60 days later. Method of measurement: Farid Wald's formula.;Serum insulin level. Timepoint: The beginning of the study and 60 days later. Method of measurement: ELISA kit.;Hemoglobin A1c. Timepoint: The beginning of the study and 60 days later. Method of measurement: ELISA kit.;Weight. Timepoint: The beginning of the study and 60 days later. Method of measurement: Digital scale.;Height. Timepoint: The beginning of the study and 60 days later. Method of measurement: Tape measure.

Secondary

MeasureTime frame
Energy intake level. Timepoint: At the beginning of the study and 60 days later. Method of measurement: 3-day Food Record Questionnaire.;Macronutrients intake level. Timepoint: At the beginning of the study and 8 weeks later. Method of measurement: 3-day Food Record Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAyda Najmi

Tabriz University of Medical Sciences

aydanjmy6@gmail.com0098 41 4793065

Outcome results

None listed

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