跳至主要内容
临床试验/RBR-10mn89c6
RBR-10mn89c6招募中Unknown

Copper IUD insertion after immediate vaginal delivery: comparison of standard technique vs. ultrasound-guided technique - a randomized double-blind study carried out in university hospital

Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo0 个研究点开始时间: 2024年2月16日最近更新:

试验速览

阶段
Unknown
状态
招募中
发起方

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

年龄范围
18Y 至 0(—)
性别
Female

入选标准

  • Pregnant women with a single fetus. Age over 18 years old. Gestational age greater than or equal to 34 weeks. Pregnant women admitted to an obstetric center in early labor (< 4 cm cervical dilation) or under labor analgesia, able to understand the study presentation, its justification and sign the informed consent form. Pregnant women expressing a desire to insert an IUD prior to the study inclusion interview

排除标准

  • Puerperal sepsis. Chorioamnionitis. Distorted uterine cavity (submucous myoma, Mullerian malformations). Cervical cancer. Fever (oral temperature = 37.8º C) during labor. Rupture of ovular membranes = 18 hours. Puerperal hemorrhage when any type of intervention is performed for puerperal hemorrhage: Manual massage, Administration of crystalloid for volume expansion or blood derivatives. Use of medications such as oxytocin, ergotamine, misoprostol, tranexamic acid. Use of intrauterine balloon. Surgical treatment such as vessel ligation and B-Lynch.

研究者

发起方
Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo

相似试验