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首页> 外文期刊>Contraception >A prospective double-blinded, randomized, placebo-controlled trial on the use of letrozole pretreatment with misoprostol for second-trimester medical abortion.
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A prospective double-blinded, randomized, placebo-controlled trial on the use of letrozole pretreatment with misoprostol for second-trimester medical abortion.

机译:前瞻性双盲,随机,安慰剂对照试验,关于来曲唑预处理和米索前列醇在孕中期药物流产中的应用。

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BACKGROUND: The aim of this randomized trial was to evaluate the abortion rate of combined regimen of letrozole and misoprostol in second-trimester abortion. STUDY DESIGN: This was a randomized, double-blinded, placebo-controlled trial of 130 women requesting legal termination of pregnancy at gestational age between 12 and 20 weeks. Letrozole 7.5 mg or placebo were given for 3 days, followed by misoprostol 400 mcg vaginally every 3 h up to a maximum of five doses on the third day. RESULTS: The abortion rate in 24 and 48 h were similar for the letrozole and placebo groups (24 h: 93.8% vs. 90.8%, respectively, p=.718; 48 h: 98.5% vs. 95.4%, respectively, p=.496). The median induction-to-abortion interval was also similar for the letrozole and placebo groups (9.6 h vs. 10.6 h, p=.145). All the side effects were comparable between the two groups. CONCLUSION: The use of letrozole pretreatment (7.5 mg daily for 3 days) with misoprostol in second-trimester abortion does not significantly improve the abortion rate of the misoprostol-only regimen.
机译:背景:这项随机试验的目的是评估孕中期流产来曲唑和米索前列醇联合方案的流产率。研究设计:这是一项随机,双盲,安慰剂对照的试验,涉及130位要求合法终止妊娠12至20周的孕妇。给予来曲唑7.5 mg或安慰剂3天,然后每3 h阴道给予米索前列醇400 mcg,第三天最多注射5剂。结果:来曲唑和安慰剂组在24 h和48 h流产率相似(24 h:分别为93.8%和90.8%,p = .718; 48 h:分别为98.5%和95.4%,p = .496)。来曲唑和安慰剂组的中位诱导至堕胎间隔也相似(9.6 h vs. 10.6 h,p = .145)。两组的所有副作用均相当。结论:在孕中期流产中使用米索前列醇来曲唑预处理(每天7.5 mg,连续3天)不能显着提高仅使用米索前列醇方案的流产率。

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