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The Effect of VitC on IVF Outcome of DOR Patients

RecruitingNAAges 20 Years - 45 YearsFemalePeking University Third Hospital
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In plain words

What the trial is, and whether it could suit you

In the context of the accelerating aging population and the continuous decline in birth rates nationwide, delaying reproductive aging in women and protecting the fertility of women of childbearing age have become urgent issues and key demands that need to be addressed in the field of maternal and child health in China. The ovaries have reproductive and hormone secretion functions and are crucial throughout the female reproductive lifecycle. Women of childbearing age in China face a serious problem of diminished ovarian reserve (DOR), which can lead to infertility, failed in vitro fertilization (IVF) treatments, miscarriage, and other adverse pregnancy outcomes, severely affecting the safety of women and their offspring. For DOR patients who desire to conceive, failure to intervene and treat promptly can result in irreversible losses and impose a significant psychological burden on them.

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Definition of DOR: Currently, there is no internationally unified standard for DOR. According to the latest POSEIDON criteria for diminished ovarian reserve (DOR), serum AMH \<1.20 ng/mL or bilateral antral follicle count (AFC) \<5 is classified as DOR. In this study, the participants are primarily DOR patients, with the following inclusion criteria: * Infertile women undergoing their 1st or 2nd IVF treatment * Diagnosed with DOR: POSEIDON criteria (AMH \<1.2 ng/mL or bilateral AFC \<5) BMI between 18.5-28.0 kg/m² * Signed informed consent Exclusion Criteria:Participants meeting any of the following criteria will be excluded from the trial: * PGT (preimplantation genetic testing) candidates * DOR caused by ovarian surgery, cancer radiotherapy/chemotherapy * Other ovulation disorders (e.g., PCOS, Cushing's syndrome, non-classic congenital adrenal hyperplasia, hyperprolactinemia) or endometriosis (chocolate cysts) * Severe thyroid disorders: Hyperthyroidism, Graves' disease, Hashimoto's thyroiditis * Acute/chronic renal insufficiency, hemodialysis, or history of severe kidney impairment * Infectious diseases: HIV, active hepatitis, metabolic acidosis, tuberculosis, etc. * Severe autoimmune diseases (e.g., rheumatoid arthritis, lupus, Crohn's disease) * Cardiovascular events within the past 3 months: Coronary artery disease/myocardial infarction/clinically significant congestive heart failure;Stroke/transient ischemic attack (TIA);Deep vein thrombosis/pulmonary embolism;Poorly controlled hypertension (SBP ≥160 mmHg or DBP ≥90 mmHg);Diagnosed diabetes mellitus;Coronary intervention (PCI) or coronary artery bypass grafting (CABG); * Neurological disorders (e.g., dementia,Alzheimer's, Parkinson's) or use of related medications * Psychiatric disorders or use of antiepileptic/antidepressant drugs * History of cancer or radiotherapy/chemotherapy * Allergy to vitamin C * Current high-dose vitamin C supplementation (\>500 mg/day) * Unwillingness to take the study-provided supplements * Alcohol abuse, smoking, or drug addiction * Participation in other clinical trials within the past month
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What it tests

  • Vitamin C
  • Placebo
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Where

6 sites
Beijing Obstetrics and Gynecology Hospital,Capital Medical University
Beijing, China
Peking university third hospital
Beijing, China
The second hospital of Hebei Medical University
Shijiazhuang, China
General Hospital of Ningxia Medical University
Yinchuan, China
Tang Du Hospital
Xi’an, China
Peking University Shenzhen Hospital
Shenzhen, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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