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临床试验/EUCTR2009-010869-23-IT
EUCTR2009-010869-23-IT进行中(未招募)不适用

Acute and long term effects of thyroid hormone replacement therapy in patients with ST-Elevation Myocardial Infarction (STEMI) and borderline/reduced triiodothyronine levels. - THIRST

OSPEDALE G.PASQUINUCCI-FONDAZIONE TOSCANA GABRIELE MONASTERIO/CNR0 个研究点开始时间: 2009年3月12日最近更新:
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试验速览

阶段
不适用
状态
进行中(未招募)
发起方

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

  • Male and female patients, all ethnic races, admitted to the Coronary Care Unit for chest pain and subsequently proven STEMI (ST Elevation Myocardial Infarction); Age between 30 to 70 years; Patients subjected to coronary revascularization through PTCA and stenting PTCA performed within 12 hours from the onset of symptoms Evidence of fT3 levels below the lower referral limit (<2.2 pg/mL for our laboratory) or decrease in fT3 plasma levels major than 20% with respect to the admission levels Signature of a written informed consent before randomization
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Previous myocardial infarction Previous evidence of compromised left ventricular function (Ejection Fraction< 40%) Hemodynamic instability, cardiogenic shock, decompensated heart failure (NYHA IV class) at admission Use of inotropic drugs Thyroid disease Patients assuming: TH replacemement therapy, anti-thyroid drugs, corticosteroids, amiodarone, oral anticoagulant therapy, oral contraceptives Patients presenting atrial fibrillation or with previous documentation of paroximal or persistent atrial fibrillation Pregnant or breast-feeding women Sever systemic diseases including: neoplasia, decompensated diabetes mellitus with glicosilated haemoglobin levels major than 9%, liver cirrhosis, chronic obstructive lung disease with moderate to severe respiratory impairment, chronic kidney failure with creatinine plasma levels major than 3 mg/dL Systemic inflammatory/ autoimmune disease Patients holding mechanical cardiac valves, pace-makers or infusion pumps, magnetic materials like metallic clips and prothesis Patients allergic to synthetic thyroid hormone or any eccipient in the drug eventually administered Patients refusing or unable to supply written informed consent.

研究者

发起方
OSPEDALE G.PASQUINUCCI-FONDAZIONE TOSCANA GABRIELE MONASTERIO/CNR

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