EUCTR2004-000108-42-GB进行中（未招募）1 期
A RANDOMISED OPEN COMPARISON OF INTRAVAGINAL APL202 (25µg) 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 MULTIPAROUS SUBJECTS.
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
- 性别
- Female
入选标准
- •1.Subjects, aged 18 years or over, having at least one previous term pregnancy suitable for induction of labour with prostaglandin cervical ripening agents.
- •2.Pregnancy duration of at least 37 weeks.
- •3.Subjects with an unfavourable cervix defined as a Bishop’s Score of less than 9 (see Appendix II)
- •4.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
- •1.Subjects who are diabetic.
- •2.Subjects with a multiple pregnancy.
- •3.Subjects in whom oxytocic drugs are generally contraindicated or where prolonged contractions of the uterus are considered inappropriate.
研究者
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