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Risk of Acute Liver Failure Among Patients With Type 2 Diabetes Exposed to Oral Antidiabetic Treatments

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Diabetes Mellitus, Type 2

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01086293
CV181-100

Details and patient eligibility

About

The purpose of this study is to compare the incidence of hospitalization with acute liver failure among patients with type 2 diabetes who are new users of Saxagliptin and those who are new users of other oral antidiabetic drugs.

Full description

Prospectively designed retrospective database study. This study will be conducted using administrative claims data and electronic medical records that are collected as part of routine clinical practice

Enrollment

113,505 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years of age or older
  • Newly prescribed Saxagliptin or an Oral Antidiabetic Drug (OAD) in a class other than Dipeptidyl peptidase IV (DPP4) inhibitors
  • Enrolled in the respective database for at least 180 days prior to the first prescription of new OAD
  • Have at least one diagnostic code for a type 2 diabetes-related condition

Exclusion criteria

  • Patients identified with a diagnostic code for acute liver failure within the 180-day baseline period
  • Patients with DPP4 inhibitor exposure during the baseline period

Trial design

113,505 participants in 2 patient groups

Patients exposed to Saxagliptin
Patients exposed to oral antidiabetic drugs (not Saxagliptin)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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