Efficacy and Safety of Shen Que (RN8) Moxibustion in Unexpected POR
Infertility
About this trial
This is an interventional treatment trial for Infertility focused on measuring Shen Que (RN8), Moxibustion, In Vitro Fertilization and Embryo Transfer (IVF-ET), Poor Ovarian Response (POR), Poseidon Criteria
Eligibility Criteria
Inclusion Criteria: ≥35 years old with normal pre-stimulation ovarian reserve parameters (antral follicle count (AFC) ≥ 5 or anti-mullerian hormone (AMH) ≥1.2 ng/ml) and with an expected poor ovarian response (fewer than 4 oocytes) after standard ovarian stimulation. Exclusion Criteria: Individuals with a Body Mass Index (BMI) ≥ 35 Kg/m2 Those using the natural cycle or mild stimulation for IVF/intracytoplasmic sperm injection (ICSI) treatment Those with a history of unilateral oophorectomy or recurrent pregnancy loss, defined as two or more spontaneous abortions Acceptors of donated oocytes or performed either In vitro Maturation (IVM) or blastocyst biopsy for Preimplantation Genetic Diagnosis (PGD) or Preimplantation Genetic Testing for Aneuploidies (PGT-A) Those previously diagnosed with congenital (e.g., mediastinal uterus and double uterus) or acquired (e.g., submucosal myoma and adenomyosis) uterine abnormalities Patients with extremely advanced age ( ≥ 45 years old) Presence of a non-surgically treated hydrosalpinx or endometrial polyp and an ovarian endometriosis cyst requiring surgery, during ovarian stimulation
Sites / Locations
- The Affiliated Hospital of Shandong University of Traditional Chinese MedicineRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Shen Que Moxibustion group
Control group