Diabetes type II. Type II diabetes (insulin independent diabetes)
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients must give their written consent to join the study voluntarily and knowingly. Patients must be diagnosed with type II diabetes with HbA1c levels between 6.5 to 7.5%. Patients must be under oral treatment with common medications to treat diabetes, such as sulfonyl urea, methformin, DPP4 inhibitors, SGLT2 inhibitors, pioglytazone. No history of autoimmune disorders. Patients must not have compromised cognitive ability. Patients may not be in any stage of pregnancy or lactation. Patients must be between 27-77 years of age.
Exclusion criteria
Exclusion criteria: Lack of a knowing and voluntary patient consent in written form. unwillingness to continue the study. Unwillingness to adhere to the project's protocols. Decision of the medical staff for any unforeseen reasons.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fasting Blood Sugar. Fasting blood sugar is generally above 125 mg/dL in type II diabetes patients. Timepoint: At the beginning of the study and 90 days after use of regular water or deuterium depleted water. Method of measurement: Blood test for fasting blood sugar.;Glycated hemoglobin, (HbA1c). Timepoint: At the beginning of the study and 90 days after use of regular water or deuterium depleted water. Method of measurement: Testing glycated hemoglobin in the blood. Glycated hemoglobin levels in type II diabetes patients is generally above 6.5%. | — |
Secondary
| Measure | Time frame |
|---|---|
| Antioxidant effects. Timepoint: At the beginning of the study and 90 days after use of regular water or deuterium depleted water. Method of measurement: Tests for malondialdehyde, catalase, glutathione peroxidase, glutathione, superoxide dismutase, and total antioxidant capacity. | — |
Countries
Iran (Islamic Republic of)
Contacts
Atomic Energy Organization of Iran