Diabetes Mellitus
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Research participants should be able to clearly understand and cooperate with all the procedures described in the Study Consent Form, including completing the questionnaires. Men and women between the ages of 20 and 75; Patients with type 2 diabetes for at least 3 years with stable glycemic control; verified by the A1c dosage in the last 3 months without change of medication.
Exclusion criteria
Exclusion criteria: Use of synthetic glucocorticoids * such as prednisone, prednisolone, methylprednisolone and hydrocortisone by oral or topical routes. Pregnancy; Type 1 Diabetes; Antecedents or suspected nephrotic syndrome, hepatic insufficiency, hyperthyroidism, acromegaly, renal failure; Use of insulin to treat diabetes
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected. | — |
Primary
| Measure | Time frame |
|---|---|
| Improvement in mean glycemia by at least 20 mg / dl in the 14 days of treatment. The average glycemia will be evaluated by the free style glucose sensor, with continuous monitoring for 14 days and downloading in specific software. | — |
Countries
Brazil
Contacts
Instituto de Ciências Farmacêuticas