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A Real World Experience of Dapagliflozin in Type 2 Diabetes

Completed
Conditions
Type2 Diabetes
Registration Number
NCT02966626
Lead Sponsor
University of Malaya
Brief Summary

Type 2 diabetes mellitus (T2DM) is creating a health pandemic globally. Management of type 2 diabetes involves combination of lifestyle intervention and drug intervention, which includes sodium-glucose transporter 2 (SGLT-2) inhibitors, such as dapagliflozin. Dapagliflozin (Forxiga®) was approved by the Malaysian Drug Authority for the treatment of type 2 diabetes in 2014. This study will describe the characteristics of patients who are prescribed dapagliflozin by diabetologists/endocrinologists in a tertiary referral center and describe their glycaemic control, weight, and renal function at baseline and during use of dapagliflozin.

Detailed Description

The prevalence of type 2 diabetes among adults \>18 years old is 17.5% in Malaysia, where half of them are undiagnosed. Diabetes also accounts for 14.5% of all-cause mortality worldwide, with close to half of the deaths are in subjects \<60 years old. These highlight the importance of early diagnosis of disease, timely intervention with appropriate therapy, and treating type 2 diabetes patients to goal to prevent the development of complications.

Asian type 2 diabetes phenotypes are different than Caucasians, i.e. significant pancreatic beta-cell dysfunction, higher visceral adiposity, more vulnerable to cardio-renal complications. Although clinical trials of SGLT-2 inhibitors have been published, real-world data on the use of this new class of antidiabetic medication is still lacking, in particularly among Asians.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
223
Inclusion Criteria
  • Diagnosis of T2DM prior to the first prescription of dapagliflozin
  • Patients with T2DM who are initiated with dapagliflozin from March 2014 till December 2015
  • Patients need to be on dapagliflozin therapy for at least six consecutive months from the index date
  • Patients need to have diabetologists/endocrinologists' follow up for at least six months after the initiation of dapagliflozin
Exclusion Criteria
  • Patients with T2DM who are initiated with dapagliflozin after December 2015
  • Patients with incomplete electronic medical records
  • Patients with Type 1 diabetes
  • Patients with latent autoimmune diabetes of adults (LADA)
  • Female Patients with T2DM who are found to be pregnant during the treatment period of dapagliflozin

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in HbA1c6 months

To assess the change in HbA1c from baseline to 6 months

Secondary Outcome Measures
NameTimeMethod
Change in body weight6 months

To assess the change in body weight from baseline to 6 months

Change in estimated glomerular filtration rate6 months

To assess the change in estimates glomerular filtration rate from baseline to 6 months

Change in albuminuria6 months

To assess the change in albuminuria from baseline to 6 months

Change in body mass index6 months

To assess the change in body mass index from baseline to 6 months

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