Study identifier:D1690R00026
ClinicalTrials.gov identifier:NCT02805283
EudraCT identifier:N/A
CTIS identifier:N/A
Direct to Patient Survey to Examine Treatment Satisfaction and Experience with Dapagliflozin Compared to Sulfonylureas
Diabetes Mellitus, Type 2
N/A
No
-
All
653
Observational
N/A
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Oct 2019 by AstraZeneca
AstraZeneca
Optum
The purpose of this study is to evaluate the diabetes related treatment satisfaction for patients with type 2 diabetes mellitus
This is a cross-sectional, observational patient survey study. Study subjects will be adult commercial members of the large US health plan affiliated with Optum with evidence of T2D initiating dapagliflozin or a sulfonylurea medication within the 3 months prior to survey mailing.
Location
Location
Eden Prairie, MN, United States
Arms | Assigned Interventions |
---|---|
Dapagliflozin, dapagliflozin/met ER Dapagliflozin cohort have at least one pharmacy claim for either dapagliflozin or dapagliflozin/metformin ER in the most recent month of pharmacy data and no pharmacy claims for a medication in the same drug class during the 6 months prior to sample identification. | - |
Sulfonylurea Sulfonylurea cohort have at least one pharmacy claim for sulfonylurea in the most recent month of pharmacy data and no pharmacy claims for a medication in the same drug class during the 6 months prior to sample identification. | - |
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