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The effect of resveratrol on diabetes treatment

The effects of Resveratrol on plasma and peripheral blood mononuclear cells (PBMCs) oxidative stress factors of type 2 diabetic patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015072523336N1
Enrollment
60
Registered
2015-08-19
Start date
2015-09-23
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

Type 2 diabetes. Non-insulin-dependent diabetes mellitus

Interventions

Sponsors

Vice chancellor of Research, Tehran University of Medical Sciences
Lead Sponsor
Diabetes Research Center, Endocrinology and Metabolism research Institute, Tehran University of Medi
Collaborator

Eligibility

Sex/Gender
All
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Ability to give informed consent; Age 40-60 years; Diabetic patients with BMI less than 35 kg/m2; Lack of insulin therapy; HbA1c > 7.5. Exclusion criteria: Subjects on any antioxidant medication; Patient on non-steroidal anti-inflammatory drug; Patients on insulin therapy; Patients with severe diabetic complications such as nephropathy , retinopathy and amputation; On any agent with significant antioxidant properties; History of alcohol abuse; Any life threatening disease such as cancer and infectious diseases; Allergy to peanuts, grapes, wine, mulberries; Pregnant women; Coronary event or procedure (myocardial infarction, unstable angina, coronary artery bypass surgery or coronary angioplasty) in the previous four weeks; Subjects on anticoagulants; History of recent taking red grapes, pistachios, almonds and berries; ALT and/or AST > 2 times above upper limit of normal.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
HbA1c. Timepoint: Before and two months after intervention. Method of measurement: HPLC.;FBS. Timepoint: Before and two months after intervention. Method of measurement: Enzymatic reaction.;Reactive oxygen species (ROS). Timepoint: Before and two months after intervention. Method of measurement: Flow cytometry.

Secondary

MeasureTime frame
HDL. Timepoint: Before and two months after intervention. Method of measurement: Spectrophotometry.;LDL. Timepoint: Before and two months after intervention. Method of measurement: Spectrophotometry.;Insulin. Timepoint: Before and two months after intervention. Method of measurement: ELISA Kit.;Cholesterol. Timepoint: Before and two months after intervention. Method of measurement: Spectrophotometry.;Triglyceride. Timepoint: Before and two months after intervention. Method of measurement: Spectrophotometry.;ALT. Timepoint: Before and two months after intervention. Method of measurement: Spectrophotometry.;AST. Timepoint: Before and two months after intervention. Method of measurement: Spectrophotometry.;Insulin resistance. Timepoint: Before and two months after intervention. Method of measurement: HOMA-IR.;CRP. Timepoint: Before and two months after intervention. Method of measurement: ELISA Kit.;Creatinine. Timepoint: Before and two months after intervention. Method of measurement: Spectrophotometry.;Urea. Timepoint: Before and two months after intervention. Method of measurement: Spectrophotometry.;BMI. Timepoint: Before and two months after intervention. Method of measurement: the formula for BMI is weight in kilograms divided by height in meters squared.;Diastolic and systolic blood pressure. Timepoint: Before and two months after intervention. Method of measurement: Sphygmomanometer and Stethoscope will be used to measure the blood pressure.;Glutathione. Timepoint: Before and two months after intervention. Method of measurement: Spectrophotometry.;Malondialdehyde (MDA). Timepoint: Before and two months after intervention. Method of measurement: Spectrophotometry.;Plasma protein carbonyl. Timepoint: Before and two months after intervention. Method of measurement: Spectrophotometry.;Total antioxidant capacity. Timepoint: Before and two months after intervention. Method of measurement: Spectrophotometry.;Expression of Sirt1. Timepoint: Before and two months after

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShadi Seyyed Ebrahimi

Tehran University of Medical Sciences

shadi_seyyedebrahimi@yahoo.com+98 21 8895 3004

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 7, 2026