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A randomized double-blind controlled trial of the use of dydrogesterone in women with threatened miscarriage in the first trimester: study protocol for a randomized controlled trial

机译:一项关于在妊娠早期使用地屈孕酮治疗先兆流产妇女的随机双盲对照试验:随机对照试验的研究方案

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摘要

BACKGROUND: Miscarriage is a common complication of pregnancy occurring in 15-20 % of all clinically recognized pregnancies. Currently, there is still no good scientific evidence to support the routine use of progestogens for the treatment of threatened miscarriage because the existing studies were not large enough to show a significant difference and some of them were not randomized or double-blind. METHODS: This is a double-blind, randomized controlled trial. A total of 400 patients presenting with first-trimester threatened miscarriage will be enrolled. They will be randomized to take dydrogesterone 40 mg per os, followed by 10 mg per os three times a day or placebo until twelve completed weeks of gestation or 1 week after the bleeding has stopped, whichever is longer. The primary outcome is the percentage of miscarriage before 20 weeks of gestation. DISCUSSION: We postulate that the dydrogesterone therapy will significantly reduce the risk of miscarriage in women with threatened miscarriage. TRIAL REGISTRATION: This study is registered at ClinicalTrials.gov, NCT02128685 . Registered on 29 April 2014.
机译:背景:流产是怀孕的一种常见并发症,占所有临床公认的妊娠的15-20%。目前,由于现有研究规模不足以显示显着差异,并且其中一些研究并非随机或双盲研究,因此尚无良好的科学证据支持常规使用孕激素治疗先兆流产。方法:这是一项双盲,随机对照试验。总共有400名患者出现了早孕先兆流产。他们将被随机分次服用dydrogesterone 40 mg / os,然后每天3次或口服安慰剂10mg / os,直到妊娠十二周或出血停止后1周,以时间较长者为准。主要结局是妊娠20周前流产的百分比。讨论:我们假设dydrogesterone治疗将显着降低先兆流产妇女的流产风险。试验注册:本研究在ClinicalTrials.gov上注册,NCT02128685。 2014年4月29日注册。

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