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临床试验/EUCTR2017-004478-32-DK
EUCTR2017-004478-32-DK进行中(未招募)1 期

The effect of metoprolol on myocardial function, hemodynamics and heart failure symptoms in patients with hypertrophic obstructive cardiomyopathy - TEMPO

Aarhus University Hospital0 个研究点目标入组 32 人开始时间: 2017年12月14日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
32

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Informed consent
  • - Symptomatic patients, who fits the criteria for HCM ( wall thickness = 15 mm in one or more myocardial segments that is not explained by loading conditions.)
  • - LVOTG > 30 mmHg at rest and/or >50 mmHg at Valsalva’s maneuver or exercise
  • - = NYHA II
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 15
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 17

排除标准

  • - Age < 18 years
  • - Know allergi to trial medication
  • - Contraindications to beta-blocker treatment
  • - Contraindications to Magnetic resonance scan including the contrast agent gadolineum
  • - Female patients who are pregnant (positive Plasma-HCG), nursing, or of childbearing potential while not practicing effective chemical contraceptive methods (i.e. oral, implanted, injectable or transdermal contraceptive hormones; intrauterine device)
  • - Pacemaker
  • - Treatment with Cordarone
  • - Atrial fibrillation/flutter at the time of examination
  • - Bradycardia < 49 beats/min
  • - Systolic blood pressure < 100 mmHg
  • - Trifasicular block
  • - Previous TASH (transcoronary ablation of septum hypertrophy) or myectomy
  • - Current abuse of alcohol and drugs
  • - Significant comorbidity or issue that makes the patient unsuitable fpr participation, judged by the investigator
  • - Patients who cannot give valid consent (e.g. mental illness or dementia)
  • - Patients who do not understand danish

研究者

发起方
Aarhus University Hospital

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