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临床试验/RBR-67h649
RBR-67h649尚未招募未知

Comparison between copper IUD (intrauterine device) and levonogestrel-releasing system immediate postpartum - randomized clinical trial

Hospital da Mulher Prof. Dr. José Aristodemo Pinotti - CAISM0 个研究点开始时间: 2018年5月16日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Intervention

入排标准

年龄范围
18Y 至 43Y(—)
性别
Female

入选标准

  • Age between 18 and 43 years; gestational age at delivery greater than or equal to 37 weeks; hemoglobin major than 8.0 during prenatal care; desire to use IUD as contraceptive method; immediate Postpartum of single gestation

排除标准

  • Diagnosis or suspicion of ovular infection; diagnosis of any other infection (anywhere); active STD (sexually transmitted disease); uterine malformation (bicorn, septate);uterine myomatosis that deforms the cavity

研究者

发起方
Hospital da Mulher Prof. Dr. José Aristodemo Pinotti - CAISM

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