Clinical Study of the Circular Motion Acupuncture Method Based on the "One Source, Three Branches" Theory for Premature Ovarian Insufficiency

Hubei Maternity and Child Health Care Hospital0 个研究点开始时间: 2026年7月31日最近更新: 2026年8月3日

适应症

试验速览

暂无简介。

•(1)Women scheduled to undergo in vitro fertilization and embryo transfer (IVF-ET) procedures and routine oocyte retrieval; (2)Residual follicular fluid samples that would otherwise be discarded after routine clinical processing can be obtained during oocyte retrieval; (3)Participants in the POI intervention group and POI control group meet the diagnostic criteria for Premature Ovarian Insufficiency (POI) or are assessed by reproductive specialists as having diminished ovarian function; (4)Participants in the non-ovarian-factor control group undergo assisted reproductive treatment due to non-ovarian factors, such as male-factor infertility or tubal-factor infertility. Female participants have normal ovarian reserve function and no confirmed POI or other reproductive endocrine disorders that may significantly affect follicular fluid test results; (5)Able to understand the study procedures, voluntarily participate in the study, and provide written informed consent.

•(1) Participants with severe diseases involving major organs or systems, including the cardiovascular, hepatic, renal, or hematopoietic systems;
•(2) Participants with malignant tumors, severe infections, or other diseases that, in the opinion of the investigators, may significantly affect the results of follicular fluid analysis;
•(3) Participants whose follicular fluid samples are obviously blood-stained, contaminated, or insufficient in volume to meet the testing requirements;
•(4) Participants with incomplete clinical data or those considered unsuitable for inclusion by the investigators.

发起方

Hubei Maternity and Child Health Care Hospital