The effect of letrozole as an adjunct in GnRH-antagonist protocol on IVF/ICSI outcome in women with endometriosis: a randomized clinical trial

IF 1.6 Q4 REPRODUCTIVE BIOLOGY Middle East Fertility Society Journal Pub Date : 2023-11-02 DOI:10.1186/s43043-023-00153-7
Maryam Farid Mojtahedi, Ashraf Moini, Ladan Kashani, Tiba Mirzarahimi
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Abstract

Abstract Background To evaluate the effect of adding letrozole to the antagonist ovarian stimulation protocol (COS) on in-vitro fertilization/intracytoplasmic sperm injection (IVF/ICSI) outcome in endometriosis patients. Methods This randomized clinical trial was carried out in the department of infertility treatment at Arash Women’s Hospital from May 2019 to May 2021. The eligible women with normal ovarian reserve tests who had endometriosis diagnosis and underwent IVF/ICSI cycles were evaluated. A flexible regimen of GnRH-antagonist protocol was used for COS. In the experimental ( n = 34), the patients received 5 mg letrozole daily for the first 5 days in combination with 150 IU of recombinant follicle-stimulating hormone (rFSH). In the control group ( n = 30), the patients received only the same dose of rFSH. The treatment cycle was compared between groups. Results Analysis of demographic characteristics, severity of endometriosis, and baseline hormonal tests of patients showed that the two groups were similar and comparable. The means of total used gonadotropins ampoules and serum E 2 level on oocyte trigger day in the letrozole group were significantly lower than those of in the control group ( P = 0.03 and P = 0.004, respectively). No statistically significant difference in terms of the total number of retrieved and MII oocytes as well as the total numbers of obtained and top-quality embryos, and cryopreserved embryos was found. Conclusion The co-treatment of letrozole with gonadotropins during the antagonist protocol was associated with a reduction in the total dose of gonadotropins, although it had no effect on the oocyte or embryo yield in patients with endometriosis. Trial registration The study was registered in the Iranian Registry of Clinical Trials on 2018 -07-13 (IRCT20150310021420N4 at www.irct.ir , registered while recruiting).
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来曲唑作为gnrh拮抗剂方案的辅助药物对子宫内膜异位症女性IVF/ICSI结果的影响:一项随机临床试验
摘要背景评价在卵巢拮抗剂刺激方案(COS)中加入来曲唑对子宫内膜异位症患者体外受精/胞浆内单精子注射(IVF/ICSI)结局的影响。方法本随机临床试验于2019年5月至2021年5月在Arash妇女医院不孕症治疗科进行。对诊断为子宫内膜异位症并接受IVF/ICSI周期的符合条件的卵巢储备检查正常的妇女进行评估。COS采用灵活的gnrh拮抗剂方案。在实验中(n = 34),患者在前5天每天服用5 mg来曲唑并联合150 IU重组促卵泡激素(rFSH)。在对照组(n = 30)中,患者仅接受相同剂量的rFSH。比较两组治疗周期。结果两组患者的人口统计学特征、子宫内膜异位症严重程度和基线激素检测结果相似且具有可比性。来曲唑组促性腺激素总使用量平均值和卵母细胞触发日血清e2水平均显著低于对照组(P = 0.03和P = 0.004)。两组的卵母细胞总数、MII卵母细胞总数、获得优质胚胎总数、冷冻保存胚胎总数均无统计学差异。结论在拮抗剂方案中,来曲唑与促性腺激素的联合治疗与促性腺激素总剂量的减少有关,尽管它对子宫内膜异位症患者的卵母细胞或胚胎产量没有影响。本研究已于2018-07-13在伊朗临床试验注册中心注册(IRCT20150310021420N4,网址为www.irct.ir,在招募时注册)。
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CiteScore
2.80
自引率
0.00%
发文量
32
审稿时长
45 weeks
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