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临床试验/TCTR20231121001
TCTR20231121001尚未招募4 期

Effects of high intensity of inspiratory muscle training in patients with heart failure with mildly reduced and preserved ejection fraction: A randomized controlled trial

Faculty of Medicine, Chulalongkorn University0 个研究点目标入组 29 人开始时间: 2023年11月21日最近更新:
适应症

试验速览

阶段
4 期
状态
尚未招募
入组人数
29

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 N/A (No limit)(—)
性别
All

入选标准

  • 1.Patients with symptoms and signs of chronic HF with a LVEF of more than 40% and no prior measurement of LVEF equal or less than 40% at baseline.
  • 2.Patients with NYHA class II or III.
  • 3.Patients with NT-pro BNP greater than 220 pg/dL or elevated LV filling pressure at rest or with exercise assessed by echocardiography.
  • 4.Patients who have been on a stable dose of HF medications for at least 4 weeks.

排除标准

  • 1.Patients who are unable to perform a baseline exercise test: gait difficulty, orthopedic problems, etc. that affect their ability to walk.
  • 2.Patients who need intravenous diuretics, vasodilators, inotropic agents, or mechanical support within a week of screening, as well as during the screening period before randomization, and have acute decompensated HF.
  • 3.Patients with recent angina or open-heart surgery within 3 months prior to randomization.
  • 4.Patients with end-stage renal disease and require renal replacement therapy or kidney transplantation
  • 5.Patients with status post-heart transplantation
  • 6.Patients with anemia (Hb less than 10 g/dl)
  • 7.Patients with significant primary moderate to severe valvular disease.
  • 8.Patients with significant primary pulmonary disease, including pulmonary arterial hypertension, chronic thromboembolic pulmonary disease or chronic obstructive pulmonary disease.
  • 9.Patients who have systemic diseases such as amyloidosis or sarcoidosis.
  • 10.Patients with any other comorbidities with life expectancy less than 1 year.

研究者

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