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The effects of rutin flavonoid on type 2 diabetes mellitus

The effects of rutin flavonoid supplement on glycemic status, lipid profile, plasma atherogenic index, brain derived neurotropic factor (BDNF), some serum inflammatory biomarkers and oxidative stress in patients with type 2 diabetes mellitus

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20151128025274N5
Enrollment
50
Registered
2020-12-30
Start date
2021-01-20
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Type 2 diabetes mellitus. Type 2 diabetes mellitus

Interventions

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Willingness to participate in the study People between 20 to 60 years old in both sexes Over at least 2 years from time of diagnosis of type 2 diabetes mellitus Body mass index (BMI) less than 35 (BMI = 35) Glycosylated hemoglobin (HbA1c) between 6.5 to 11%

Exclusion criteria

Exclusion criteria: Reluctance of patients to participate in the study Developing complications from diabetes such as kidney failure Diabetic patients taking insulin Thyroid disease Anemia Pregnancy, lactation Traveling more than 2 weeks Smokers Use of other dietary supplements, probiotics and anti-inflammatory drugs Use of any antioxidant supplements in the last 3 months Use of immunosuppressive drugs Following of special diets other than the diet specific to diabetic patients Change of diet or decide to lose weight

Design outcomes

Primary

MeasureTime frame
Fasting blood sugar. Timepoint: Before and after the intervention. Method of measurement: Using enzymatic kit method.

Secondary

MeasureTime frame
Insulin. Timepoint: Before and after the intervention. Method of measurement: ELISA.;HbA1C. Timepoint: Before and after the intervention. Method of measurement: By HPLC method and with Ds5 device.;HOMA -IR. Timepoint: Before and after the intervention. Method of measurement: [FPG (mmol / l x FPI (FIU/ml)] / 22.5.;QUICKi. Timepoint: Before and after the intervention. Method of measurement: 1 / [log (I0) + log (G0)] ISQUICKi.;Plasma atherogenic index. Timepoint: Before and after the intervention. Method of measurement: log TG/HDL.;HDL-c. Timepoint: Before and after the intervention. Method of measurement: Using enzymatic kit method.;Triglyceride. Timepoint: Before and after the intervention. Method of measurement: Using enzymatic kit method.;LDL.C. Timepoint: Before and after the intervention. Method of measurement: Using enzymatic kit method.;Total cholestrol. Timepoint: Before and after the intervention. Method of measurement: Using enzymatic kit method.;IL-6. Timepoint: Before and after the intervention. Method of measurement: ELISA.;TAC. Timepoint: Before and after the intervention. Method of measurement: ELISA.;MDA. Timepoint: Before and after the intervention. Method of measurement: ELISA.;BDNF. Timepoint: Before and after the intervention. Method of measurement: ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHadi Bazyar

Ahvaz University of Medical Sciences

hadibazyar2015@gmail.com+98 61 3333 0747

Outcome results

None listed

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