首页> 外文OA文献 >Effects of a Chinese Patent Medicine Gushen’antai Pills on Ongoing Pregnancy Rate of Hormone Therapy FET Cycles: A Multi-Center, Randomized, Double-Blind, Placebo-Controlled Clinical Trial
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Effects of a Chinese Patent Medicine Gushen’antai Pills on Ongoing Pregnancy Rate of Hormone Therapy FET Cycles: A Multi-Center, Randomized, Double-Blind, Placebo-Controlled Clinical Trial

机译:中国专利医学甘肃 - 塔伊丸对持续妊娠期妊娠率的影响:多中心,随机,双盲,安慰剂控制的临床试验

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摘要

In the past decade, the number of frozen-thawed embryo transfer (FET) has increased dramatically with the expansion of surgical indications and the improvement of freezing related technologies. How to improve the success rate and reduce the adverse effects of FET is our research priorities. This study aimed to investigate the safety and effectiveness of Gushen’antai pills (GSATP) by measuring the ongoing pregnancy rate (OPR) in patients from FET and hormone therapy (HT) cycle. From November 2019 to May 2020, 5 Chinese hospitals conducted a multi-center, randomized, double-blind, placebo-controlled study. In total, 271 HT FET cycles in patients were randomly divided (1:1 ratio) to receive GSATP (6 g, tid) or placebo (6g, tid) for 12 weeks of pregnancy. Patients, clinicians, and researchers were blinded to treatment allocation. The primary endpoint was the OPR at week 12 of pregnancy. The secondary endpoints were vaginal bleeding or brown discharge rate, implantation rate (IR), clinical pregnancy rate (CPR) and abortion rate (AR). Adverse events were recorded during the treatment period. The results showed that the OPR remained higher in the GSATP group when compared to placebo group (56.62% vs. 44.44%, p = 0.045). Vaginal bleeding or brown discharge rate was lower in the GSATP group than the placebo group (10% vs. 23.08%, p = 0.032), while the IR (35.16% vs. 27.64%, p = 0.070), CPR (58.82% vs. 48.15%, p = 0.078), incidence of total adverse events (8.09% vs. 3.22%, p = 0.051) and AR (3.75% vs. 7.69%, p = 0.504) were similar between GSATP and placebo groups. Subgroup analysis showed that there were significant differences in CPR (74.19% vs. 54.17%, p = 0.004) and OPR (72.04% vs. 51.04%, p = 0.003) between GSATP group and Placebo group when the patient was younger than 35 years old. This multi-center, randomized, double-blinded, placebo-controlled clinical study showed for the first evidence that GSATP may have potential to improve the OPR and decrease vaginal bleeding or brown discharge rate in HT FET cycle patients.
机译:在过去的十年中,冻融胚胎移植(FET)的数量已经与手术适应证的扩大和冻结相关技术的改进大幅提升。如何提高成功率,降低FET的不利影响,是我们研究的重点。本研究旨在通过测量从FET和激素治疗(HT)周期患者持续妊娠率(OPR)调查Gushen'antai丸(GSATP)的安全性和有效性。从十一月到2019年2020年5,5级中国的医院进行的多中心,随机,双盲,安慰剂对照研究。总体上,患者271个HT FET周期随机分为(1:1的比例),以接收GSATP(6克,TID)或安慰剂(6克,TID)治疗12周妊娠。患者,临床医生和研究人员都不清楚治疗的分配。主要终点是在怀孕第12周的OPR。次要终点是阴道出血或棕色放电率,着床率(IR),临床妊娠率(CPR)和流产率(AR)。不良事件在治疗期间的记录。结果表明,与安慰剂相比,组(56.62%对44.44%,P = 0.045)时,OPR仍然是GSATP组中更高。阴道出血或棕色放电率比安慰剂组的GSATP组低(10%比23.08%,P = 0.032),而IR(35.16%对27.64%,P = 0.070),CPR(58.82%对。48.15%,p = 0.078),总不良事件发生率(8.09%对3.22%,p = 0.051)和AR(3.75%对7.69%,p = 0.504)为GSATP和安慰剂组之间是相似的。亚组分析表明,有在CPR GSATP组和安慰剂组之间的差异显著(74.19%对54.17%,P = 0.004)和OPR(72.04%对51.04%,P = 0.003),当患者年轻超过35年老的。这种多中心,随机,双盲,安慰剂对照的临床研究表明,第一个证据GSATP可能有潜力改善OPR,减少阴道出血或褐色分泌物率HT FET周期的患者。

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