Diabetes Mellitus, Type 2
Conditions
Keywords
Diabetes Mellitus, Type 2 Diabetes, Acarbose (25/50mg) and Metformin (500mg) in fixed dose combination
Brief summary
The study is designed as non interventional to collect data on the safety especially, severe hypoglycemia or documented symptomatic hypoglycemic episodes and effectiveness of acarbose/metformin fixed-dose combination under real-life treatment condition in large sample of type-2 diabetes patients in India. The study objective is to evaluate severe hypoglycemia or documented symptomatic or asymptomatic hypoglycemic events reported as adverse events. The study will begin after the study approval by ethics committee. All patients with type 2 diabetes on acarbose or metformin monotherapy and prescribed Glucobay M will be included in study after taking the informed consent. Patients will be observed for up to 24 weeks (2 weeks).The study involves general examination of patients, collection of data like history of disease, concomitant medication, drug dose etc. The study is planned to enroll 10000 subjects from multiple study centers spread across India. The study data will be analyzed with appropriate statistical methods.
Interventions
DRUGAcarbose/Metformin (Glucobay M, BAY81-9783)
Acarbose (25/50mg) and Metformin (500mg) in fixed dose combination.
Sponsors
Bayer
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
* Patient will be enrolled after the decision to administer acarbose/metformin fixed dose combination for type-2 diabetes management has been made by the attending physician on the basis of best clinical practice and patient needs. * Willing to give informed consent for participating in this study
Exclusion criteria
* Patients receiving anti-diabetic medication other than acarbose, or metformin monotherapy at the time of enrollment in the study will be excluded. However, during observation period, any additional anti-diabetics medication administered by the attending physician will be allowed & recorded in case record form. * Patient receiving acarbose/metformin fixed dose combination during 3-months prior to enrollment. *
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of severe hypoglycemia or documented symptomatic or asymptomatic hypoglycemic events reported as adverse events | 24 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Mean change in body weight | baseline and 24 weeks |
| Incidence of adverse events other than hypoglycemia reported | 24 weeks |
| Mean change in HbA1c level | baseline and 24 weeks |
| Mean change in fasting blood sugar | baseline and 24 weeks |
| Mean change in serum LDL(low-density lipoprotein) cholesterol | baseline and 24 weeks |
| Mean change in serum triglyceride | baseline and 24 weeks |
| Mean change in serum HDL (High density lipoproteins) cholesterol | baseline and 24 weeks |
| Change in percent satisfaction to the therapy from baseline as measured by 5 point satisfaction scale | baseline and 24 weeks |
| Number of patient with adverse event (Tolerability) | Baseline and 24 weeks |
| Mean change in postprandial blood sugar | baseline and 24 weeks |
Outcome results
None listed