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临床试验/ISRCTN10972090
ISRCTN10972090已完成未知

Induction of labor with a balloon catheter versus oral misoprostol following term pre-labor rupture of membranes – a randomized controlled trial

Helsinki University Central Hospital0 个研究点目标入组 180 人开始时间: 2021年2月5日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
180

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • 1. Aged =18 years
  • 2. Primiparous or multiparous women with singleton pregnancy
  • 3. Gestational age =37 weeks (term)
  • 4. Spontaneous rupture of membranes without the onset of labor within 18-48 h
  • 5. Unfavorable cervix (Bishops score <6)
  • 6. Cephalic presentation of fetus
  • 7. No colonization of Group B Streptococcus on vaginal and rectal swab

排除标准

  • 1. Pre-term pre-labor rupture of membranes (<37 gestational weeks)
  • 2. Clinical signs of infection (such as vaginitis, chorionamnionitis)
  • 3. Active infection or carrier of human immunodeficiency virus (HIV), hepatitis B, or hepatitis C
  • 4. Type 1 diabetes
  • 5. Group B Streptococcal colonization of vagina and/or rectum (detected by swab test)
  • 6. Any acute condition, maternal or fetal, requiring the immediate delivery of the fetus
  • 7. Intrauterine growth restriction
  • 8. Macrosomia or weight estimation =4.5 kg
  • 9. Fetus in any other presentation than cephalic (such as breech or transverse)
  • 10. Previous caesarean section or any other uterotomy (such as myomectomy)
  • 11. Insufficient understanding or language deficiency to comprehend the patient guide and consent form
  • 12. Refusal of participation or refusal for signed consent

研究者

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