Comparative Analysis of Cost-effectiveness Between Sulfonylureas and DPP4 Inhibitors in Combination With Metformin in Treatment of Type 2 Diabetic Patients : A Retrospective, Observational Study.
- Conditions
- Type 2 Diabetes Mellitus (T2DM), Cost-effectiveness, Sulfonylureas, DPP4 Inhibitors, Metformin
- Interventions
- Drug: sulfonylurease with metformin, DPP4 inhibitors with Metformin
- Registration Number
- NCT06570980
- Lead Sponsor
- Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
- Brief Summary
The aim of this study is to compare the cost effectiveness of Sulfonylureas and DPP4-inhibitors in combination with Metformin among type2 diabetic patients diagnosed for 2-5 years. Glycemic status and other clinical outcome are compared in between two groups and ICER are compared.
- Detailed Description
Type 2 diabetes mellitus (T2DM) is a highly prevalent chronic disease. Every 3 in 4 adults have diabetes in low and middle income countries. Diabetes costs about 966 billion USD dollars in total health expenditure. This is a huge economic burden for low and middle income countries, where people have to pay out of their pocket for medical expense. Type2 Diabetes is responsible for various serious life threatening complications like cardiovascular death, retinopathy, nephropathy, stroke etc.
Along with diet and exercise, lifelong pharmacotherapy is needed. But cost of drug is increasing day by day, especially newer agents are very much expensive. The aim of this study is to compare the cost and effectiveness of Metformin plus sulfonylureas with Metformin plus DPP4 inhibitors in management of type 2 diabetic patient. This research will be conducted in Pharmacology department of Bangabandhu Sheikh Mujib Medical University (BSMMU), outpatient department of BIRDEM General Hospital, and Siddhirganj diabetic center, Narayanganj from the day of approval by IRB to July, 2024. It will be multi centered, retrospective, observational, cost-effectiveness study. It will involve type 2 diabetic patients who have diagnosed for 2 years and taking either any of sulfonylurease or DPP4 inhibitors along with Metformin. 206 patients will be enrolled, 103 in each group. One group will who are taking sulfonylureas with Metformin and another group will who are taking DPP4 inhibitors with Metformin. Primary outcome will be glycemic control which will be measured by HbA1c % and secondary outcome will be cardiovascular events like hypertension, angina, myocardial ischemia for which ECG and patients medical record will be analyzed, nephropathy will be classified by eGFR, insulin therapy and any hospitalization needed or not. Data will be collected about various socio-demographic variables such as age, sex, education, family history of diabetes, other co morbidities. Hypertension with diabetes will be considered in equal percentage in both groups. Total direct medical cost like drug price, hospitalization and cost of adverse drug reaction will be measured which will be actual medical cost of individual patient. Then cost-effectiveness analysis will be done by ICER. Descriptive statistics will be used for demographic variables. Means \& standard deviation for ii continuous variables and number \& percentage for categorical variables will be used. T test can be used to compare cost in two groups. Chi-square test may be used to compare clinical outcome. Price of drug will be obtained from BDNF 5th edition for particular brand of above mentioned drug in every individual patient. This study will revealed whether there is significant difference in healthcare costs and clinical outcome between the above mentioned two groups. This retrospective study will provide valuable insight about cost effectiveness of sulfonylureas and DPP4 inhibitors for the management of T2DM. Healthcare providers even policymakers can be benefitted to take informed decision in patient care and formulary choices.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 200
- New onset type2 diabetes mellitus diagnosed for 2 -5 years.
- Taking either sulfonylurea or DPP4 inhibitors combined with Metformin from the time of diagnosis.
- Age 18 years or above.
- Both male and female.
- Provided written informed consent.
- Unwillingness to participate or unwillingness to give written informed consent.
- Patients on Insulin therapy or monotherapy with metformin since the time of diagnosis.
- Taking other than sulfonylurea or DPP4 inhibitors combined with Metformin from the time of diagnosis.
- Diabetes related complications at the time of diagnosis.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Group A- type 2 diabetic patients having sulfonylurease with metformin sulfonylurease with metformin, DPP4 inhibitors with Metformin Sulfonylurease- gliclazide(30/60/80mg), glimepiride (1/2/3/4mg), glibenclamide (5mg), glipizide (5mg) metformin - 500/850/1000mg Group B- type 2 diabetic patients having DPP4 inhibitors with metformin sulfonylurease with metformin, DPP4 inhibitors with Metformin DPP4 inhibitors- Linagliptin (2.5/5mg), Sitagliptin (50mg), Vildagliptin (50mg) metformin - 500/850/1000mg
- Primary Outcome Measures
Name Time Method HbA1c% 2-5years achievment of target HbA1 less than 7%
- Secondary Outcome Measures
Name Time Method nephropathy 2-5years development of nephropathy
3rd line therapy 2-5years addition of any 3rd drug
Insulin therapy 2-5years requirement of insulin therapy
hospitalization 2-5years requirement of hospitalization
Trial Locations
- Locations (1)
BSMMU
🇧🇩Dhaka, Bangladesh