跳至主要内容
临床试验/EUCTR2004-000107-18-GB
EUCTR2004-000107-18-GB进行中(未招募)1 期

A RANDOMISED OPEN COMPARISON OF INTRAVAGINAL APL202 (25 or 50µg) FOLLOWED BY 25µg AFTER 4 AND 8 HOURS VERSUS 3mg OF DINOPROSTONE AS A VAGINAL TABLET FOLLOWED BY 3mg AFTER 6 HOURS IN THE INDUCTION OF LABOUR IN NULLIPAROUS SUBJECTS.

Alliance Pharmaceuticals0 个研究点目标入组 415 人开始时间: 2005年5月3日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
415

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

  • -Nulliparous subjects, aged 18 years or over, with a singleton pregnancy suitable for induction of labour with prostaglandin cervical ripening agents.
  • -Pregnancy duration of at least 37 weeks.
  • -Subjects with an un-favourable cervix defined as a Bishop’s Score of less the 9.
  • -Signed informed consent.
  • 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
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • -Subjects who are diabetic.
  • -Subjects with a multi-fetal pregnancy.
  • -Subjects in whom oxytocic drugs are generally contraindicated or where prolonged contractions of the uterus are considered inappropriate.

研究者

相似试验