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临床试验/NCT02299609
NCT02299609Unknown不适用

Therapeutic Effect of Ultrasound Beams as an Adjunct to Reperfusion Therapy in STEMI

Sakarya University2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2013年1月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
100
试验地点
2
主要终点
Increase in left ventricular function

研究概览

简要总结

Successfully perfused STEMI patients will receive routine transthoracic echocardiography qid for 4 days or placebo. Myocardial function and infarct size will be evaluated at 3 and 6 months.

详细描述

Patients who had acute STEMI and successfully reperfused by either thrombolytic therapy or primary angioplasty and stenting will be included this study.

A basal routine echocardiography will be obtained in all patients after reperfusion therapy. Thereafter, patients will be divided into two groups: 1.Treatment group will receive transthoracic echocardiography using Philips HD11 XE ® for 30 minutes qid for 4 days. 2. Placebo group will have the same Philips HD11 XE ® echo transducer applied for the same time and duration on their chest but with the ultrasound turned-off. Detailed left and right ventricle function as well as performance index and stress-strain imaging will be obtained and analyzed at 3 and 6 months.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients presenting within 12 hours of their first ST- elevation myocardial infarction that is successfully reperfused; and completed baseline echocardiographic evaluation and accepted participation in the study

排除标准

  • With prior ST- elevation myocardial infarction
  • Patients presenting >12hrs
  • Not successfully reperfused
  • Not completed baseline ECHO evaluation,
  • Not accepting participation in the study

结局指标

主要结局

Increase in left ventricular function

时间窗: At 3 and 6 months

Ultrasound beams during echocardiography application expected to ameliorate the left ventricle function

次要结局

  • Decrease in infarct size(At 3 and 6 months)

研究者

发起方
Sakarya University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ramazan Akdemir

Prof. Ramazan Akdemir, MD

Sakarya University

研究点 (2)

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