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Clinical Trial Details

Trial ID: L7075
Source ID: NCT04295005
Associated Drug: Empagliflozin
Title: A Study Based on Data From German Sick Funds That Looks at the Costs of Treatment of Type-2 Diabetic Patients With Empagliflozin vs. DPP-4 Inhibitors vs. GLP-1 Receptor Agonists
Acronym:
Status: COMPLETED
Study Results: YES
Results: https://ClinicalTrials.gov/show/NCT04295005/results
Conditions: Diabetes Mellitus, Type 2
Interventions: DRUG: Empagliflozin|DRUG: DPP-4i|DRUG: GLP-1-RA
Outcome Measures: Primary: Direct Healthcare Cost, The direct healthcare cost is reported, including inpatient cost, outpatient cost, medication cost, and total cost. Patients starting Empagliflozin (EMPA) versus either Dipeptidyl peptidase 4 inhibitor (DPP-4i), Sitagliptin (SITA) or Glucagon-like peptide-1 receptor agonist (GLP-1-RA) were matched 1:1 based on a propensity score using a nearest-neighbor matching algorithm without replacement and a maximum caliper of 0.001. The propensity scores were derived by logistic regression models estimating the probability of a patient belonging to the different treatment groups (three estimations: EMPA versus DPP-4i, EMPA versus SITA, and EMPA versus GLP-1-RA). The cost per observed patient year is calculated as the sum of the cost/ sum of the observed time \[year\] over all patients. Final values were rounded to the nearest digit., Dataset included all adult persons, who were continuously insured between 01 january 2014 until 31 december 2018 (except for death), approximately a 4 year period.|Healthcare Resource Utilization, Healthcare resource utilization includes hospitalizations, hospital stays. outpatient visits, and rehabilitation stays., Dataset included all adult persons, who were continuously insured between 01 january 2014 until 31 december 2018 (except for death), approximately a 4 year period. | Secondary: Indirect Healthcare Costs (Including Indirect Costs of Days Absent From Work), Indirect healthcare costs (including indirect costs of days absent from work) includes indirect costs for hospitalization, outpatient visits, absent from work, and rehabilitation stays., Dataset included all adult persons, who were continuously insured between 01 january 2014 until 31 december 2018 (except for death), approximately a 4 year period.
Sponsor/Collaborators: Sponsor: Boehringer Ingelheim
Gender: ALL
Age: CHILD, ADULT, OLDER_ADULT
Phases:
Enrollment: 24500
Study Type: OBSERVATIONAL
Study Designs: Observational Model: |Time Perspective: p
Start Date: 2020-11-16
Completion Date: 2021-09-30
Results First Posted: 2024-08-30
Last Update Posted: 2024-08-30
Locations: Boehringer Ingelheim, Ingelheim am Rhein, 55216, Germany
URL: https://clinicaltrials.gov/show/NCT04295005