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临床试验/NCT03794518
NCT03794518Unknown3 期

Effect of Combination Therapy With Dapagliflozin Plus Low Dose Pioglitazone on Hospitalization Rate in Patients With Heart Failure and Preserved Left Ventricular Ejection Fraction

Hamad Medical Corporation1 个研究点 分布在 1 个国家目标入组 648 人开始时间: 2019年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
入组人数
648
试验地点
1
主要终点
Time to first hospitalization for heart failure after starting intervention

研究概览

简要总结

The prevalence of type 2 diabetes mellitus (T2DM) in Qatar and nations worldwide has increased in recent decades into epidemic proportions. Cardiovascular (CVD) disease is the leading cause of death in T2DM patients. Approximately 80% of T2DM patients will die because of CV cause. Congestive heart failure (CHF) is a major cause of CV death in T2DM, and it also is responsible for significant morbidity and health care expenditure due to high rate of hospitalization for heart failure.

详细描述

Community based studies have demonstrated similar prevalence of HF with reduced ejection fraction (HFpEF) and HF with reduced LV function (HFrEF) in patients hospitalized for CHF. Moreover, the prevalence of HFrEF is declining over the past two decades, whereas that of HFpEF is progressively increasing. Progressive increase in obesity and T2DM prevalence is likely among the principal factors responsible for the steady increase in HFpEF prevalence.

The aims of the present study are to examine whether therapies that correct the myocardial metabolic abnormalities present in subjects with T2DM and diastolic dysfunction improve myocardial diastolic dysfunction and reduce the rate of hospitalizations in patients with HFpEF

The primary objective of the study is to examine the effect of combination therapy with pioglitazone (15 mg) plus dapagliflozin (10 mg) versus placebo on hospitalization for heart failure in patients with HFpEF.

Eligible subjects, who consent for participating in the study, will be seen by the study coordinator. Medical history and physical examination will be performed. Each subject will receive the following measurements:

Medical history and physical examination including weight, height, waist, blood pressure and pulse.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Participant)

盲法说明

Random process

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

  • Diagnosis of type 2 diabetes according to the ADA criteria.
  • Drug naïve or on stable dose of antidiabetic therapy (oral agents and/or insulin) for 3 months preceding recruitment.
  • Hospitalized for HFpEF (defined as hospitalization require intravenous diuresis) in the 6 months preceding recruitment.
  • eGFR >60 ml/min
  • Presence of LV diastolic dysfunction in echocardiography
  • We have limited the inclusion criteria in the present study to T2DM patients with HFpEF and evidence of diastolic dysfunction by echocardiography in order to select a homogenous group of HFpEF patients with similar etiology, likely "metabolic HFpEF". We believe that this subgroup of HFpEF will benefit most from treatment with low dose pioglitazone (15 mg) plus dapagliflozin (10 mg).

排除标准

  • Treatment with pioglitazone or SGLT2 inhibitor in the 3 months prior to recruitment.
  • eGFR < 60 ml/min
  • LVEF <50%;
  • Valvular heart disease, ASD, VSD
  • Chronic lung disease
  • diabetes mellitus type 1
  • patients with acute coronary syndrome, stroke or transient ischemic attack in the preceding 6 months
  • pregnancy or lactation period

研究组 & 干预措施

Pioglitazone Plus dapaglifliozin

Experimental

Pioglitazone 15mg and dapaglifliozin 10mg together in T2DM patients having HF and HFpEF conditions

干预措施: Pioglitazone Plus dapaglifliozin (Drug)

Placebo

Placebo Comparator

Beta blockers, ACEI, ARB, and aldosterone

干预措施: Placebo (Drug)

结局指标

主要结局

Time to first hospitalization for heart failure after starting intervention

时间窗: 3 years

Hospitalization for heart failure will be defined as a hospitalization \>24 hours requiring intravenous diuretic infusion.

次要结局

  • Number of all cause mortality(3 years)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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