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临床试验/NCT04419337
NCT04419337招募中2 期

Comparison of Combined Pioglitazone and SGLT2 Inhibitors vs. DPP4 Inhibitors in Diabetic Patients With Ischemic Stroke: Rationale and Study Design

Chang Gung Memorial Hospital1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2019年9月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
200
试验地点
1
主要终点
HbA1C

研究概览

简要总结

Introduction: An optimal combination of antidiabetic drugs for diabetic patients with ischemic stroke is not well-established. The objective of this randomized trial is to evaluate whether combination of pioglitazone and a sodium glucose cotransporter 2 (SGLT-2) inhibitor, compared with a dipeptidyl peptidase-4 (DPP-4) inhibitor, reduces recurrent stroke in diabetic patients with recent ischemic stroke.

Methods and analysis: The trial is a randomized, parallel-group study conducted at 7 hospitals in Taiwan. Inclusion criteria are adult patients with a history of ischemic stroke within 3 months, diabetes mellitus with Hba1C > 7%, taking metformin currently or previously, and estimated glomerular filtration rate ≥ 45 mL/min/1.73 m2. Eligible patients who sign the informed consent forms will be randomly assigned in a 1:1 ratio to receive either combination of pioglitazone and an SGLT2 inhibitor (empagliflozin or dapagliflozin or canagliflozin) vs. a DPP4 inhibitor. Primary outcome is change in HbA1C between 6 months and baseline in active vs comparator groups. Additional biomarker outcomes are change in hs-CRP insulin resistance, B type natriuretic peptide, and urine albumin creatinine ratio between 6 months and baseline.

Ethics and dissemination Study protocol was approved by the Institutional Review Board of Chang Gung Memorial Hospital, Chiayi Branch, Taiwan (201702353A3, 201802340A3 and 201902176A3). All participants will be required to sign and date an informed consent form. Study findings will be disseminated via a peer-reviewed journal.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Ischemic stroke within 3 months of randomization
  • Type 2 diabetes mellitus and Hba1C > 7.0% and under metformin therapy currently or previously
  • Estimated glomerular filtration rate (eGFR) ≥ 45 mL/min/1.73 m2
  • Age ≥ 20 y at study entry
  • Ability and willingness to provide informed consent

排除标准

  • History of congestive heart failure (NYHA class 1-4)
  • History of bladder cancer
  • History of repeated (> 2 episodes) urinary tract infection or genital tract infection
  • Irreversible medical conditions with predicted survival < 1 years
  • Current use of an insulin
  • Current use of a glucagon-like peptide-1 receptor agonist
  • Current use of pioglitazone or an SGLT-2 inhibitor

研究组 & 干预措施

Active arm

Experimental

metformin+pioglitazone+an SGLT2 inhibitor

干预措施: Metformin plus Pioglitazone plus an SGLT2 inhibitor (Drug)

Control arm

Active Comparator

metformin + DPP4 inhibitors

干预措施: Metformin plus Pioglitazone plus an SGLT2 inhibitor (Drug)

结局指标

主要结局

HbA1C

时间窗: 6 months from baseline in active vs control arms

blood test to evaluate glycemic control

次要结局

  • UACR(6 months from randomization in active vs control arms)
  • hs-CRP(6 months from randomization)
  • NT-proBNP(6 months from randomization)
  • insulin resistance(6 months from randomization)

研究者

发起方
Chang Gung Memorial Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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