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Melatonin in Assisted Reproductive Technology: A Pilot Double-Blind Randomized Placebo-Controlled Clinical Trial

机译:辅助生殖技术中的褪黑素:一项双盲随机安慰剂对照临床试验

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摘要

>Purpose: To explore in a small pilot study whether oral melatonin, administered during ovarian stimulation increases clinical pregnancy rate (CPR) after IVF and what dose might be most effective.>Methods: Pilot double-blind, dose-finding, placebo-controlled randomized clinical trial in private IVF clinics in Australia between September 2014 and September 2016. One hundred and sixty women having their first cycle of IVF or ICSI were randomized to receive placebo (n = 40), melatonin 2 mg (n = 41), melatonin 4 mg (n = 39), or melatonin 8 mg (n = 40) twice per day (BD) during ovarian stimulation. The primary outcome was CPR. Secondary outcomes included serum and follicular fluid (FF) melatonin concentrations, oocyte/embryo quantity/quality, and live birth rate (LBR). Analysis was performed using the intention-to-treat principle.>Results: There was no difference in CPR or LBR between any of the four groups (p = 0.5). When all the doses of melatonin were compared as a group with placebo, the CPR was 21.7% for the former and 15.0% for the latter [OR 1.57 (95% CI 0.59, 4.14), p = 0.4]. There were also no differences between the groups in total oocyte number, number of MII oocytes, number of fertilized oocytes, or the number or quality of embryos between the groups. This is despite mean FF melatonin concentration in the highest dose group (8 mg BD) being nine-fold higher compared with placebo (P < 0.001).>Conclusion: No significant differences were observed in CPR or oocyte and embryo parameters despite finding a nine-fold increase in FF melatonin concentration. However, this study was not sufficiently powered to assess differences in CPR and therefore, these results should be interpreted with caution. Because this was a small RCT, a beneficial effect of melatonin on IVF pregnancy rates cannot be excluded and merits confirmation in further, larger clinical trials. ANZCTR ( Project ID: ACTRN12613001317785).
机译:>目的:在一项小型先导研究中探讨在卵巢刺激过程中口服褪黑激素是否会增加试管受精后的临床妊娠率(CPR),以及最有效的剂量。>方法: 2014年9月至2016年9月间,在澳大利亚的私家IVF诊所进行了双盲,剂量确定,安慰剂对照的随机临床试验。将160名首次试管婴儿或ICSI周期的妇女随机接受安慰剂(n = 40 ),卵巢刺激期间每天两次(BD)褪黑激素2 mg(n = 41),褪黑激素4 mg(n = 39)或褪黑激素8 mg(n = 40)。主要结果是心肺复苏。次要结果包括血清和卵泡液(FF)褪黑激素浓度,卵母细胞/胚胎数量/质量和活产率(LBR)。使用意向性治疗原则进行分析。>结果:四组中的任何一组之间的CPR或LBR均无差异(p = 0.5)。当将所有剂量的褪黑素与安慰剂组进行比较时,前者的CPR为21.7%,后者为15.0%[OR 1.57(95%CI 0.59,4.14),p = 0.4]。两组之间的卵母细胞总数,MII卵母细胞数量,受精卵母细胞数量或胚胎数量或质量之间也没有差异。尽管最高剂量组(8 mg BD)的FF褪黑素浓度平均比安慰剂高9倍(P <0.001)。>结论:在CPR或卵母细胞和尽管发现FF褪黑素浓度增加了9倍,但胚胎参数却没有变化。但是,这项研究不足以评估CPR的差异,因此,应谨慎解释这些结果。由于这是一个很小的RCT,因此无法排除褪黑激素对IVF妊娠率的有益作用,并且值得进一步的大型临床试验证实。 ANZCTR(项目ID:ACTRN12613001317785)。

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