Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 2:32 PM
Ignite Modification Date:
2025-12-24 @ 2:32 PM
NCT ID:
NCT02577159
Eligibility Criteria:
Inclusion Criteria:
* Male or female subjects with type 2 diabetes mellitus of from 20 to 65 years of age.
* Patients who have not achieve the clinical target of the glycemic control (less than 7.0% in HbA1c).
* Patients who received the diet therapy, the exercise therapy or the following anti-diabetic drugs in addition to the diet and/or exercise therapy (up to two drugs) with dosage stable for 8 weeks prior to entry.
* Sulfonylurea (Glymepiride 2mg/day or less, Glibenclamide 1.25mg/day or less, Gliclazide 40mg/day or less)
* Thiazolidine (Actos)
* Biguanide (Metformin, Buformin)
* alpha-glucosidase inhibitor (Voglibose, Miglitol, Acarbose)
* DPP4 inhibitors (Sitagliptin, Linagliptin, Anagliptin, Teneligliptin, Alogliptin, Saxagliptin)
* Informed consent to participate in the study prior to any study procedures.
Exclusion Criteria:
* Type 1 diabetes mellitus
* Moderate or severe renal dysfunction (eGFR\<45 ml/min/1.73m2 or hemodialysis)
* Severe hepatic insufficiency (AST and/or ALT \>3x upper limit of normal)
* Adrenal insufficiency or pituitary gland dysfunction
* Malnourishment, starvation, irregular dietary intake, poor dietary intake, debilitating condition or a severe muscle movement
* Volume depleted patients; concomitant medication such as loop diuretics.
* Excessive alcohol intake (\>60g daily)
* SGLT2 inhibitors such as dapagliflozin are already administered
* Contraindication with dapagliflozin
* Start a new medication of statins, fibrates, ezetimibe or probucol within a month
* Females who are likely to be pregnant, during pregnancy or lactating
* Participants in other clinical trials
* Inability to communicate and comply with all study requirements.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
20 Years
Maximum Age:
65 Years
Study:
NCT02577159
Study Brief:
Protocol Section:
NCT02577159