低分子肝素对冷冻胚胎移植中反复植入失败的中国妇女妊娠结局的影响:一项双盲、随机、安慰剂对照试验。

IF 2.4 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Minmin Cao, Wenjing Wan, Yaxuan Zhang, Yan Zhao, Anmiao Sun, Shanshan Gao, Linlin Cui, Wenting Wang
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引用次数: 0

摘要

导论:在世界范围内进行体外受精和胚胎移植的患者中,复发性植入失败(RIF)的发生率可高达10%。然而,低分子肝素(LMWH)在RIF中的临床疗效仍然存在争议。目前,缺乏高质量的临床研究来验证低分子肝素治疗RIF患者的有效性,特别是在冷冻胚胎移植(FET)周期中。因此,本随机对照试验旨在研究低分子肝素对接受FET治疗的RIF妇女妊娠结局的影响。方法与分析:本前瞻性、单中心、双盲、随机、安慰剂对照临床试验将在中国山东大学第二医院进行。将招募414名年龄≤40岁、正在接受FET周期的RIF女性,并将其随机分配到研究组(低分子肝素)或对照组(安慰剂)。仅转移第5天或第6天的一个囊胚,且Gardner形态学评分≥4bc。从移植之日起,每天给予低分子肝素4000-6000 IU或安慰剂皮下注射。主要结果是活产率。次要结局包括临床妊娠率、生化妊娠率、胚胎着床率、早期流产率、持续妊娠率、异位妊娠率、妊娠相关并发症、围产期并发症、胎儿出生体重、先天性畸形等不良反应。伦理与传播:本方案获得山东大学齐鲁医学院第二医院伦理委员会批准(KYLL-2023-442)。研究结果将在同行评议的出版物中传播。试验注册号:中国临床试验注册中心,ChiCTR2400083577。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of low-molecular-weight heparin on pregnancy outcomes in Chinese women with recurrent implantation failure undergoing frozen embryo transfer: a double-blind, randomised, placebo-controlled trial.

Introduction: The incidence of recurrent implantation failure (RIF) can reach up to 10% among patients undergoing in vitro fertilisation and embryo transfer worldwide. However, the clinical efficacy of low-molecular-weight heparin (LMWH) in RIF remains a subject of controversy. Currently, there is a lack of high-quality clinical research validating the effectiveness of LMWH in treating patients with RIF, particularly during frozen embryo transfer (FET) cycles. Therefore, this randomised controlled trial aimed to investigate the impact of LMWH on pregnancy outcomes in women with RIF undergoing FET.

Methods and analysis: This prospective, single-centre, double-blind randomised, placebo-controlled clinical trial will be conducted in the Second Hospital of Shandong University, China. A total of 414 women with RIF, aged ≤40 years, who are undergoing FET cycles will be recruited and randomly assigned to the study group (LMWH) or the control group (placebo). Only one blastocyst which is from day 5 or day 6 and has a Gardner morphology score ≥4 BC will be transferred. LMWH 4000-6000 IU per day or placebo will be administered by subcutaneous injection from the day of transplantation. The primary outcome is the live birth rate. The secondary outcomes include the clinical pregnancy rate, biochemical pregnancy rate, embryo implantation rate, early miscarriage rate, ongoing pregnancy rate, ectopic pregnancy rate, pregnancy-related complications, perinatal complications, fetal birth weight, congenital malformations and other adverse reactions.

Ethics and dissemination: The protocol received approval from the Ethics Committee of the Second Hospital, Cheeloo College of Medicine, Shandong University (KYLL-2023-442). The findings will be disseminated in peer-reviewed publications.

Trial registration number: Chinese Clinical Trial Registry, ChiCTR2400083577.

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来源期刊
BMJ Open
BMJ Open MEDICINE, GENERAL & INTERNAL-
CiteScore
4.40
自引率
3.40%
发文量
4510
审稿时长
2-3 weeks
期刊介绍: BMJ Open is an online, open access journal, dedicated to publishing medical research from all disciplines and therapeutic areas. The journal publishes all research study types, from study protocols to phase I trials to meta-analyses, including small or specialist studies. Publishing procedures are built around fully open peer review and continuous publication, publishing research online as soon as the article is ready.
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