Clinical Trials Logo

Clinical Trial Summary

To compare, by insulin use at the index date, the incidence of hospitalization for acute liver injury (ALI) among patients with type 2 diabetes mellitus who are new users of dapagliflozin with those who are new users of antidiabetic drugs (ADs) in classes other than sodium-glucose cotransporter 2 (SGLT2) inhibitors, insulin monotherapy, metformin monotherapy, or sulfonylurea monotherapy.


Clinical Trial Description

The overall goal of this research study is to estimate the risk of hospitalization for acute liver injury in patients who are prescribed dapagliflozin compared to patients prescribed other specific oral antidiabetic drugs. Dapagliflozin and other antidiabetic drugs are used to treat type 2 diabetes mellitus. Because of the mechanism of action for dapagliflozin and results from small safety monitoring studies, there is interest in further evaluating the safety of dapagliflozin in large populations. The study will be implemented in three administrative health care data sources in two countries: in the United Kingdom, the Clinical Practice Research Datalink (CPRD); and in the United States, the Centers for Medicare and Medicaid Services (CMS) Medicare databases and the HealthCore Integrated Research Database (HIRDSM). Individuals in the databases will be included in the study if they meet the following age criteria; 18 years and older (CPRD and HIRD), or 65 years or older (Medicare); and if they did not have type 1 diabetes, are new users of one of the study drugs and meet the criteria of at least 180 days of electronic data before their first prescription of the study drug. The study period starts July 1, 2013 in CPRD, January 1, 2014 in PHARMO and January 9, 2014 in the United States data sources, and will end at the latest available data at each database at the time of analysis ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02695095
Study type Observational
Source AstraZeneca
Contact
Status Completed
Phase
Start date January 1, 2017
Completion date November 30, 2020

See also
  Status Clinical Trial Phase
Active, not recruiting NCT02833064 - Biomarkers in Liver Failure
Completed NCT04913298 - Prospective Study for the Application of Cytosorb® in Critically Ill Patients N/A
Completed NCT01548690 - Safety Study of Ornithine Phenylacetate to Treat Patients With Acute Liver Failure/Severe Acute Liver Injury Phase 2
Recruiting NCT03204591 - Bacterial Infections in Cirrhotic Patients With Acute Severe Liver Injury
Completed NCT00518440 - A Multi-Center Trial to Study Acute Liver Failure in Adults
Completed NCT03667157 - Liver Function After Intravenous Methylprednisolone Administration Phase 4
Recruiting NCT04862221 - TReatment for ImmUne Mediated PathopHysiology Phase 2
Not yet recruiting NCT06103981 - Acute Liver Injury in Patients With Pneumonia