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临床试验/CTIS2024-512407-39-00
CTIS2024-512407-39-00进行中(未招募)1 期

Beta-blockeRs tO patieNts with CHronIc Obstructive puLmonary diseasE (BRONCHIOLE) - BRONCHIOLE-2017

Region Oerebro Laen0 个研究点目标入组 1,700 人开始时间: 2024年6月19日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
1,700

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 至 65+(—)
性别
All

入选标准

  • A diagnosis of COPD confirmed by spirometry showing post bronchodilator value of Forced Expiratory Volume in one second (FEV1)//Forced Vital Capacity (FVC) <70 according to the Global Initiative on Obstructive Pulmonary Disease (GOLD), and with a history of tobacco smoking or occupational/environmental exposure for smoke gas or dust, =40 years of age, Sinus rhythm =50/min and <120 at inclusion, Written informed consent

排除标准

  • Known hypersensitivity to metoprolol or related derivatives, Systolic blood pressure <90 mmHg, Severe bronchial asthma, Current beta-blocker treatment, Inability to provide informed consent, Age below 40 years, Acute on-going exacerbation of COPD, Previous randomization in the BRONCHIOLE trial, Ongoing pregnancy (excluded by pregnancy test in fertile women), AV block II or III unless treated with a pacemaker, Sinus bradycardia (resting heart rate <50/min), Sick sinus syndrome unless treated with a pacemaker, Atrial fibrillation/flutter (AF), Clinical signs of or a previous diagnosis of left-sided heart failure (HF), angina pectoris (AP), myocardial infarction (MI), cerebrovascular disease or critical peripheral ischemia, Systolic blood pressure <90 mmHg, Any tachyarrythmias other than sinus rhythm, Sinustachycardia >120 / min

研究者

发起方
Region Oerebro Laen

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