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临床试验/NCT07669623
NCT07669623尚未招募不适用

Effects of Different Acupuncture Techniques on the Success Rate in Patients With Recurrent Implantation Failure

Cui Hong Zheng1 个研究点 分布在 1 个国家目标入组 312 人开始时间: 2026年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
312
试验地点
1

研究概览

简要总结

To conduct a multi-center, randomized, controlled clinical study aimed at formally evaluating the impact of different acupuncture methods on the success rate in patients with recurrent implantation failure

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 39 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Meets the criteria for RIF diagnosis (≥ 3 instances of unsuccessful transfer of high-quality embryos).
  • Age: < 40 years.
  • Planning for a cycle involving the transfer of frozen-thawed embryos (FET).
  • Possession of a transplantable frozen blastocyst (≥3BB).
  • Endometrial thickness >7 mm within the period of endometrial transformation.

排除标准

  • Individuals planning to undergo preimplantation genetic diagnosis (PGD).
  • Recipients of egg donations.
  • Chromosomal abnormalities in either spouse or one partner (excluding chromosomal polymorphisms).
  • Patients with known embryo-related factors leading to implantation failure.
  • Abnormalities of the uterus that may affect implantation (including uterine malformations, uterine tuberculosis, submucosal myomas, severe uterine adhesions, severe uterine endometriosis, myomas with a diameter of ≥4 cm, and so on).
  • Those with significant abnormalities in immunity or coagulation.
  • Individuals with other endocrine disorders, such as thyroid disorders, hyperprolactinemia, insulin resistance, diabetes, and adrenal disorders, whose hormone levels have not been well-controlled over the past 3 months.
  • Individuals with untreated hydrosalpinx;
  • Individuals with a Body Mass Index (BMI) below 18 and above 25 kg/ m
  • Men with severe abnormalities in semen quality.
  • Individuals with a history of needle phobia.
  • Individuals who have previously participated in this study or received acupuncture treatment within the past three months;
  • Any other conditions deemed unsuitable for participation by the researchers.

研究组 & 干预措施

placebo acupuncture group

Placebo Comparator

nonpenetrating placebo needles

干预措施: Placebo Group (Device)

acupuncture group 1

Experimental

indwelling intradermal needles

干预措施: acupuncture group 1 (Device)

acupuncture group 2

Experimental

combining fire needle and regular acupuncture

干预措施: acupuncture group 2 (Device)

研究者

发起方
Cui Hong Zheng
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Cui Hong Zheng

Clinical professor, principal investigator

Huazhong University of Science and Technology

研究点 (1)

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