跳至主要内容
临床试验/EUCTR2005-001034-32-GB
EUCTR2005-001034-32-GB进行中(未招募)1 期

Does pre-operative Sildenafil protect against pulmonary related complications following cardiopulmonary bypass? A randomised trial in children undergoing cardiac surgical repair

HS Greater Glasgow, Yorkhill0 个研究点目标入组 24 人开始时间: 2006年1月27日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
24

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

入选标准

  • Inclusion criteria
  • - pediatric patients undergoing open heart surgery utilising cardiopulmonary bypass to correct acyanotic congenital heart disease
  • - age >3 months
  • - parents that show a good understanding of their child's condition and are happy for their child to participate in the study
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Exclusion criteria
  • - patients with known organ dysfunction prior to surgery (pulmonary, renal or hepatic)
  • - communication barriers resulting in poor basic comprehension of the proposed study (e.g. language barrier)
  • - patients with cyanotic heart disease
  • -patients undergoing heart surgery without the use of cardiopulmonary bypass
  • - patients who do not tolerate oral Sildenafil (e.g. Vomiting) or whose surgery is subsequently cancelled

研究者

发起方
HS Greater Glasgow, Yorkhill

相似试验