Study identifier:D169AR00015
ClinicalTrials.gov identifier:NCT05932901
EudraCT identifier:N/A
CTIS identifier:N/A
A multinational, observational, secondary data study describing management and treatment with dapagliflozin in routine clinical practice among patients with chronic kidney disease
Chronic Kidney Disease
N/A
No
-
All
2682052
Observational
18 Years - 130 Years
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Apr 2024 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Dapagliflozin 10mg initiators Adult patients (aged ≥18 years) with chronic kidney disease, who received a dapagliflozin 10mg prescription on or after the country-specific CKD indication approval date, and who did not previously have a prescription for dapagliflozin. | - |
Dapagliflozin 10mg eligible but untreated Adult patients (aged ≥18 years) with chronic kidney disease, who meet the country-specific approved dapagliflozin 10mg treatment criteria for CKD on or after the local CKD indication approval date, but have not received a prescription | - |
Incident CKD Adults patients (aged ≥18 years) who newly meet the CKD definition (diagnosis or laboratory indication) during the study period. | - |