跳至主要内容
临床试验/EUCTR2011-005979-16-ES
EUCTR2011-005979-16-ES进行中(未招募)1 期

PREECLAMPSIA OF PREVENTION IN PATIENTS THROUGH ovodonation aspirin in early gestation

Instituto de Investigación Sanitaria La Fe0 个研究点目标入组 136 人开始时间: 2012年9月14日最近更新:
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
136

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

性别
Female

入选标准

  • Patients over 18 years. - Patients receiving oocyte donation. - Patients who have
  • become pregnant. - Single or multiple gestations. - To accept the conditions of the
  • study by signing the appropriate informed consent
  • single pregnancies
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 372
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Known allergy to ASA. - History of peptic ulcer. - Use of prostaglandin inhibitors
  • within 10 days before the start of the study. - History of chronic renal disease,
  • thyroid, liver or heart disease. - Psychiatric or cognitive pathology that prevents the
  • understanding of the conditions of informed consentKnown allergy to ASA. - History of peptic ulcer. - Use of prostaglandin inhibitors
  • within 10 days before the start of the study. - History of chronic renal disease,
  • thyroid, liver or heart disease. - Psychiatric or cognitive pathology that prevents the
  • understanding of the conditions of informed consent

研究者

发起方
Instituto de Investigación Sanitaria La Fe

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