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临床试验/EUCTR2013-005336-23-GB
EUCTR2013-005336-23-GB进行中(未招募)1 期

Outcome After Selective Early Treatment for Closure of Patent Ductus Arteriosus in Pre-term Babies - Baby-OSCAR Trial

niversity of Oxford0 个研究点目标入组 730 人开始时间: 2015年6月12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)
入组人数
730

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

  • Babies will be considered eligible for inclusion into the study if they are;
  • Born at 23+0 to 28+6 weeks of gestation
  • Less than 72 hours old
  • Confirmed by echocardiography to have a large PDA which
  • oIs = 1.5 mm in diameter (determined by gain optimised colour Doppler)
  • oHas unrestrictive pulsatile left to right flow
  • In addition:
  • The responsible clinician is uncertain about whether this baby might benefit from treatment to close the PDA
  • Written informed consent has been obtained from the parent(s)
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range 0
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range 0

排除标准

  • Babies will be excluded from participation in the study if they have;
  • No realistic prospect of survival
  • Severe congenital anomaly
  • Structural heart disease requiring treatment
  • Other conditions that would contraindicate the use of ibuprofen (intracranial or gastrointestinal haemorrhage, coagulopathy, thrombocytopenia (platelet count <50,000), renal failure, pulmonary hypertension, known or suspected necrotising enterocolitis)
  • Antenatal treatment with a COX inhibitors
  • Received indomethacin, ibuprofen or paracetamol after birth.

研究者

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