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.
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
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