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临床试验/NCT03895411
NCT03895411Unknown4 期

Multicenter Clinical Study of Therapeutic Effect of Sotalol on Children With Arrhythmia (Paroxysmal Supraventricular Tachycardia, Paroxysmal Atrial Tachycardia, Ventricular Tachycardia, Idiopathic Ventricular Tachycardia, Premature Ventricular Contraction ) in Children Aged From 0d to 14 Yrs

Shengjing Hospital1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2019年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
入组人数
500
试验地点
1
主要终点
QT interval of ECG

研究概览

简要总结

This study aims to investigate the efficacy and safety of oral sotalol alone or combination with other anti-arrhythmic medicines in the treatment of arrhythmias in children. The study will regularly monitor the Holter, electrocardiogram (ECG), Echocardiography (Echo), blood routine, urine routine, serum ion, liver and kidney function, troponin I, hypersensitive troponin T, N-terminal pro-brain natriuretic peptide (NT pro-BNP), etc, before and after receive sotalol therapy. Compare the degree of arrhythmia improvement in patients and the side effects after oral sotalol.

详细描述

Monitoring the Holter, ECG, Echocardiography , blood routine, urine routine, serum ion, liver and kidney function, troponin I, hypersensitive troponin T, NT pro-BNP beforehand. Eligible patients should stop all anti-arrhythmia drugs and digitalis, tricyclic antidepressants, beta blockers or calcium antagonists for at least 5 half-lives, and then do Holter. Randomly grouped. Judging the results according to the situation before and after oral sotalol.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
— 至 14 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Age 0 day to 14 year-old
  • Diagnosis of tachycardia (paroxysmal supraventricular tachycardia, paroxysmal atrial tachycardia, ventricular tachycardia, idiopathic ventricular tachycardia, premature ventricular contraction) and had an episode within 3 months; Premature Ventricular Contractions (PVC) (total 10000 times/d, or>5000 times/d with multiple source PVC, or total > 3000 times/d but with paired PVC+ multiple source PVC, or ventricular tachycardia);
  • Although PVC≤ 10000 times/d, but there are obvious symptoms such as palpitation, chest tightness, fatigue, dizziness and other symptoms that need improvement.
  • Signed informed consent before the trial
  • Good compliance

排除标准

  • Heart failure that is ineffective in conventional treatment;
  • Left ventricular ejection fraction (LVEF) ≤ 50%;
  • Suffering from bronchial asthma;
  • Resting sinus heart rate (HR) in newborns <90 bpm; -8 yrs <80 bpm; ≥ 8 yrs <60 bpm;
  • Corrected QT Interval (QTc) ≥ 450ms;
  • II ° -III ° atrioventricular block (AVB);
  • Severe liver, renal dysfunction, acute myocardial infarction, acute myocarditis, electrolyte imbalance have not been corrected;
  • The child has undergone major surgery in the past 4 weeks;
  • The child has participated in other clinical trials in the past 4 weeks;
  • The child has digestive, nervous, circulatory, kidney or liver disease

研究组 & 干预措施

Sotalol

Experimental

Oral sotalol 2.5mg/kg/time, per 12h. Combination therapy: betaloc

干预措施: sotalol (Drug)

Sotalol

Experimental

Oral sotalol 2.5mg/kg/time, per 12h. Combination therapy: betaloc

干预措施: betaloc (Drug)

Propafenone

Active Comparator

Oral Propafenone 5mg/kg/time, pre 8h Combination therapy: betaloc

干预措施: Propafenone (Drug)

Propafenone

Active Comparator

Oral Propafenone 5mg/kg/time, pre 8h Combination therapy: betaloc

干预措施: betaloc (Drug)

结局指标

主要结局

QT interval of ECG

时间窗: 3 month

次要结局

  • Hemoglobin(1 week, 3 month)
  • Aspertate aminotransferase (AST)(1 week, 3 month)
  • Blood pressure(1 week, 3 month)
  • Wed Blood Cell (WBC)(1 week, 3 month)
  • Platelet(1 week, 3 month)
  • Creatinine(1 week, 3 month)
  • Red Blood Cell (RBC)(1 week, 3 month)
  • Albumin(1 week, 3 month)
  • Alanine aminotransferase (ALT)(1 week, 3 month)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Hong Wang

Professor

Shengjing Hospital

研究点 (1)

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