ITMCTR2200006462招募中1 期
Clinical efficacy of WYHZ formula on maternal-fetal interface microenvironment and embryo implantation in patients with chronic endometritis combined with recurrent implantation failure
试验速览
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional study
入排标准
- 年龄范围
- 25 至 40(—)
- 性别
- Female
入选标准
- •1) Be between the ages of 25-40 years.
- •2) meeting the diagnostic criteria for CE and RIF.
- •3) TCM evidence consistent with spleen and kidney yang deficiency and internal dampness.
- •4) having transferable D3-day high-quality frozen embryos (7-9 embryonic cells on day 3 after fertilization, 10% fragmentation, with stage-stage specific cell size and no multinucleation) or frozen blastocysts (=3BB).
- •5) estrogen and progestin replacement therapy (HRT) with an endometrial thickness of =7 mm on the day of endometrial transformation.
- •6) voluntarily subjected to the trial and agreed to sign the informed consent form.
排除标准
- •1) Those who are ready to undergo PGD.
- •2) Those receiving donor eggs.
- •3) chromosomal abnormalities (excluding chromosomal polymorphisms) in both or one of the spouses.
- •4) Patients with known embryonic factors leading to implantation failure.
- •5) uterine pathologies that may affect implantation (including uterine malformations, uterine tuberculosis, history of uterine adhesions, submucosal fibroids, adenomyosis, >4 cm interstitial myomas)
- •6) recurrent spontaneous abortion (2 or more fetal losses before 28 weeks of gestation)
- •7) combined with other endocrine disorders such as thyroid disease, hyperprolactinemia, insulin resistance, diabetes mellitus, adrenal disease, etc., with poorly controlled hormone levels in the last 3 months
- •(8) clearly diagnosed autoimmune diseases such as systemic lupus erythematosus, rheumatoid arthritis, antiphospholipid syndrome, etc.
- •9) those with untreated hydrocele in the fallopian tubes
- •10) Those who are allergic to the drugs in this study.
研究者
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