首页> 外文期刊>Trials >Efficacy and safety of levothyroxine (L-T4) replacement on the exercise capability in chronic systolic heart failure patients with subclinical hypothyroidism: Study protocol for a multi-center, open label, randomized, parallel group trial (ThyroHeart-CHF)
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Efficacy and safety of levothyroxine (L-T4) replacement on the exercise capability in chronic systolic heart failure patients with subclinical hypothyroidism: Study protocol for a multi-center, open label, randomized, parallel group trial (ThyroHeart-CHF)

机译:左甲状腺素(L-T4)替代对亚临床甲状腺功能减退的慢性收缩性心力衰竭患者运动能力的功效和安全性:一项多中心,开放标签,随机,平行分组试验(ThyroHeart-CHF)的研究方案

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Subclinical hypothyroidism is a common condition in patients with heart failure and is defined as elevated serum thyroid hormone (TSH) with normal circulating free thyroxine (FT4). Evidence on the effect of thyroid hormone treatment is lacking. We designed a randomized controlled trial to compare the efficacy and safety of thyroid hormone supplementation in patients with chronic heart failure complicated with subclinical hypothyroidism. Eligible participants were identified from the cardiology units of five study centers based on the following criteria: 18?years or older, systolic heart failure with NewYork Heart Association (NYHA) class II–III, left ventricular ejection fraction ≤?40%, and subclinical hypothyroidism (TSH 4.78μIU/ml, ?10 μIU/ml?+?FT4 level within reference range). Eligible patients will be randomly assigned in a 1:1 manner to receive thyroxine replacement therapy plus standard chronic heart failure (CHF) treatment or only standard CHF therapy. Levothyroxine will be administered at an initial dose of 12.5?μg once daily and will be titrated until TSH is within the normal range. The primary endpoints include the difference in distance of the six-minute walk test between 24?weeks and baseline. The secondary endpoints include differences in plasma NT-proBNP levels and serum lipid profiles, changes in the NYHA classification, cardiovascular death, re-hospitalization, differences in echocardiographic and cardiac magnetic resonance imaging measures, and Minnesota Living With Heart Failure Questionnaire (MLHFQ) results between 24?weeks and baseline. ThyroHeart-CHF is designed as a prospective, multi-center, randomized, controlled clinical trial to study the efficacy and safety of thyroid hormone supplementation in patients with chronic heart failure complicated with subclinical hypothyroidism. The study findings will have significant implications for discovering the new therapeutic targets and methods of heart failure. ClinicalTrials.gov, NCT03096613 . Registered on 30 March 2017.
机译:亚临床甲状腺功能减退症是心力衰竭患者的常见疾病,定义为血清甲状腺激素(TSH)升高和正常循环甲状腺素(FT4)。缺乏有关甲状腺激素治疗效果的证据。我们设计了一项随机对照试验,以比较补充甲状腺激素在慢性心力衰竭合并亚临床甲状腺功能减退症患者中的疗效和安全性。根据以下标准从五个研究中心的心脏病科中识别出合格的参与者:18岁以上,纽约心脏协会(NYHA)II-III级收缩性心力衰竭,左心室射血分数≤?40%以及亚临床甲状腺功能减退(TSH>4.78μIU/ ml,<?10μIU/ ml?+?FT4水平在参考范围内)。符合条件的患者将以1:1的方式随机分配,接受甲状腺素替代治疗加标准慢性心力衰竭(CHF)治疗或仅标准CHF治疗。左甲状腺素的初始剂量为每天12.5μg,每天一次,将被滴定直至TSH在正常范围内。主要终点包括24周与基线之间六分钟步行测试的距离差异。次要终点包括血浆NT-proBNP水平和血清脂质谱的差异,NYHA分类的变化,心血管死亡,再次住院,超声心动图和心脏磁共振成像方法的差异以及明尼苏达州心衰患者问卷调查(MLHFQ)的结果在24周到基线之间。 ThyroHeart-CHF设计为一项前瞻性,多中心,随机,对照的临床试验,旨在研究补充甲状腺激素在慢性心力衰竭并发亚临床甲状腺功能减退症患者中的有效性和安全性。该研究结果将对发现心力衰竭的新治疗靶点和方法具有重要意义。 ClinicalTrials.gov,NCT03096613。 2017年3月30日注册。

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