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临床试验/CTRI/2017/12/010725
CTRI/2017/12/010725
尚未招募
未知

Comparative evaluation of the three point of care testing devices; Thromboelastograpgh (TEG), Rotational-thromboelastometer (ROTEM) and Sonoclot analyzer in cyanotic congenital cardiac surgery: a correlation with routine laboratory tests and postoperative bleeding.

DST0 个研究点目标入组 0 人待定

概览

阶段
未知
干预措施
未指定
疾病 / 适应症
Health Condition 1: null- Cyanotic Congenital Heart Disease
发起方
DST
状态
尚未招募
最后更新
4年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
待定
最后更新
4年前
研究类型
Observational

研究者

发起方
DST

入排标准

入选标准

  • Patients of either gender aged between one to 50 years, undergoing elective cardiac surgery for cyanotic congenital heart disease will be included in this study.

排除标准

  • 1\.Patients on preoperative anticoagulants
  • 2\.Patients with known coagulopathy
  • 3\.Patients undergoing redo surgery
  • 4\.Patients undergoing cardiac surgery without involving CPB will not be included in the study.

结局指标

主要结局

未指定

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