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基于转录组的子宫内膜容受性评估(Tb-ERA)在中国复发性植入失败(RIF)患者中的临床有效性:一项前瞻性随机对照试验的研究方案。

The clinical efficiency of transcriptome-based endometrial receptivity assessment (Tb-ERA) in Chinese patients with recurrent implantation failure (RIF): A study protocol for a prospective randomized controlled trial.

作者信息

Zhang Wen-Bi, Li He, Lu Xiang, Chen Jun-Ling, Li Lu, Chen Jiu-Cheng, Wu Han, Sun Xiao-Xi

机构信息

Shanghai Ji Ai Genetics & IVF Institute, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, 200011, China.

Unimed Biotech (Shanghai) Co., Ltd., Shanghai, China.

出版信息

Contemp Clin Trials Commun. 2022 May 28;28:100928. doi: 10.1016/j.conctc.2022.100928. eCollection 2022 Aug.

Abstract

BACKGROUND

Today, approximately 10% of participants in assisted reproductive technology (ART) are defined as having recurrent implantation failure (RIF). Recent studies show that endometrial receptivity array can improve pregnancy and implantation rates by nearly 20% in women with RIF. However, these studies are limited, with little published data in the Chinese population. Recently, we have established a transcriptome-based endometrial receptivity assessment (Tb-ERA) method of predicting the endometrial window of implantation (WOI) using transcriptome-profiling data of different phases of the menstrual cycle from healthy fertile Chinese women by RNA-Seq. It is meaningful to conduct a randomized controlled trial (RCT) to assess the clinical efficiency of Tb-ERA in Chinese patients with RIF.

METHODS

In this RCT, a total of 200 RIF patients will be recruited and randomized into 2 groups. Patients in the Tb-ERA group will undergo a Tb-ERA test, after which embryo transfer time will be adjusted according to Tb-ERA results and embryo transfer will be performed again in the next cycle. Patients in the control group will not receive any interventions until the next transfer cycle. We will perform statistical analysis on both groups at the primary endpoint (clinical-pregnancy rate) and at secondary endpoints (rate of WOI displacement, embryo implantation, biochemical pregnancy, early abortion, and ectopic pregnancy). : This study aims to evaluate the effectiveness of our Tb-ERA test in Chinese RIF patients and to determine that whether Tb-ERA could improve the clinical-pregnancy rate in these RIF patients.

TRIAL REGISTRATION

NCT04497558, registered August 4, 2020.

摘要

背景

如今,辅助生殖技术(ART)中约10%的参与者被定义为反复植入失败(RIF)。最近的研究表明,子宫内膜容受性阵列可使RIF女性的妊娠率和植入率提高近20%。然而,这些研究存在局限性,在中国人群中发表的数据很少。最近,我们建立了一种基于转录组的子宫内膜容受性评估(Tb-ERA)方法,通过RNA测序,利用健康可育中国女性月经周期不同阶段的转录组分析数据来预测子宫内膜着床窗(WOI)。开展一项随机对照试验(RCT)以评估Tb-ERA在中国RIF患者中的临床疗效具有重要意义。

方法

在这项RCT中,总共将招募200名RIF患者并随机分为两组。Tb-ERA组的患者将接受Tb-ERA检测,之后根据Tb-ERA结果调整胚胎移植时间,并在下一周期再次进行胚胎移植。对照组的患者在下一移植周期前不接受任何干预。我们将在主要终点(临床妊娠率)和次要终点(WOI移位率、胚胎植入、生化妊娠、早期流产和异位妊娠)对两组进行统计分析。本研究旨在评估我们的Tb-ERA检测在中国RIF患者中的有效性,并确定Tb-ERA是否能提高这些RIF患者的临床妊娠率。

试验注册

NCT04497558,于2020年8月4日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22c0/9163422/884c9b255d02/gr1.jpg

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