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临床试验/NCT04098575
NCT04098575已完成不适用

Treatment of T2DM Patients in Germany Receiving Empagliflozin: A Retrospective RWE Study Description of Treatment and Population Characteristics of Type 2 Diabetic Patients in Germany Receiving Empagliflozin: A Retrospective Real-World Evidence (RWE) Study Based on German Registries DPV&DIVE

Boehringer Ingelheim1 个研究点 分布在 1 个国家目标入组 9,571 人开始时间: 2019年9月16日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
9,571
试验地点
1
主要终点
Percentage of Participants With Antidiabetic and Cardiovascular Co-medication

研究概览

简要总结

Description of the real-life treatment of adult patients with type-2 diabetes mellitus (T2DM) receiving Empagliflozin, comparing the characteristics of patients starting Empagliflozin in three time intervals

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • At least two outpatient T2DM diagnoses (ICD E11.-) in two different quarters and/or at least one inpatient T2DM diagnosis (ICD E11)
  • At least one prescription of an empagliflozin-containing antidiabetic drug: Jardiance® (Empagliflozin, ATC A10BK03, former A10BX12) or Synjardy® (Empagliflozin/ Met¬for¬min, ATC A10BD20)

排除标准

  • Any diagnosis of T1DM

研究组 & 干预措施

Patients receiving Empagliflozin until mid Sep 2015

Patients receiving Empagliflozin before the EMPA-REG-OUTCOME study was published time until mid-Sept. 2015; Cohort 1

干预措施: Empagliflozin (Drug)

Patients receiving Empagliflozin until CV Label Change time

Patients receiving Empagliflozin starting from the EMPA-REG-OUTCOME study being published until CV Label Change time from mid-Sept. 2015-mid-Jan. 2017; Cohort 2

干预措施: Empagliflozin (Drug)

Patients receiving Empagliflozin until last available data cut

Patients receiving Empagliflozin starting from mid-Jan. 2017 until last; Cohort 3

干预措施: Empagliflozin (Drug)

结局指标

主要结局

Percentage of Participants With Antidiabetic and Cardiovascular Co-medication

时间窗: At baseline.

Percentage of participants with antidiabetic and cardiovascular co-medication, including lipid-lowering agents, other antihypertensives, antiplatelets and anticoagulants.

Percentage of Participants With Previous Occurence of Cardiovascular Comorbidities

时间窗: At baseline.

Percentage of patients with previous occurence of cardiovascular (CV) comorbidities, including myocardial infarction, stroke, coronary artery disease, peripheral arterial disease, congestive heart failure.

Percentage of Participants With Previous Occurence of Other Typical Diabetes Complications

时间窗: At baseline.

Percentage of participants with previous occurence of other typical diabetes complications, including, Neuropathy, Nephropathy, Chronic Kidney Disease, Microalbuminuria, Macroalbuminuria, estimated glomerular filtration rate (eGFR), diabetic foot syndrome, retinopathy (background and proliferative).

次要结局

  • Percentage of Participants With Previous Glucose-lowering Treatment(At baseline.)
  • Percentage of Participants by Age Category(At baseline.)
  • Percentage of Male Participants(At baseline.)
  • Weight of Participants(At baseline.)
  • Height of Participants(At baseline.)
  • Glycated Hemoglobin (HbA1c)(At baseline.)
  • Duration of Diabetes(At baseline.)
  • Percentage of Patients Participated in Disease Management Programme (DMP) Type 2 Diabetes(At baseline.)
  • Number of Participants With Hospitalizations(At baseline.)
  • Dosage of Empagliflozin(At baseline.)
  • Fasting Plasma Glucose (FPG)(At baseline.)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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