[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"ovarian-response\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:ovarian-response":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,42],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":4},"100053495","the-effects-of-coenzyme-q10-pretreatment-on-ovarian-function-and-assisted-reproductive-outcomes-in-patients-with-ovarian-hyporesponsiveness-100053495",false,"NCT07260773","The Effects of Coenzyme Q10 Pretreatment on Ovarian Function and Assisted Reproductive Outcomes in Patients With Ovarian Hyporesponsiveness.","The Effects of Coenzyme Q10 Pretreatment on Ovarian Function and Assisted Reproductive Outcomes in Patients With Poor Ovarian Response: A Single-Center Randomized Controlled Trial","Inclusion Criteria:\n\n* Individuals seeking IVF-ET fertility treatment;\n* Meeting the Bologna criteria for the definition of poor ovarian response (POR), specifically:\n* (1) Meeting 2 of the following 3 criteria:\n* ① Presence of high-risk factors for POR;\n* ② Previous cycle with ≤3 retrieved oocytes under a standard stimulation protocol;\n* ③ Abnormal ovarian reserve assessment: Antral follicle count (AFC) \\\u003C5 or Anti-Müllerian hormone (AMH) \\\u003C1.1 ng\u002FmL.\n\nor\n\n* (2) Patients with normal age or ovarian reserve function who experience poor ovarian response (POR) after two consecutive cycles of maximum ovarian stimulation protocols;\n* BMI between 18.5-28.0 kg\u002Fm²\n* Voluntarily participate and sign an informed consent form.\n\nExclusion Criteria:\n\n* Age ≥40 years;\n* Baseline FSH \\>25 U\u002FL;\n* Endocrine disorders (e.g., diabetes, thyroid disease) or autoimmune diseases (e.g., rheumatoid arthritis, lupus, Crohn's disease), chromosomal abnormalities, uterine malformations;\n* History of ovarian surgery; history of uterine surgery; adenomyosis;\n* History of more than 3 cycles of controlled ovarian stimulation (COS);\n* Male infertility;\n* Use within the past 3 months of medications that may affect ovarian reserve or ovarian responsiveness (e.g., oral contraceptives, glucocorticoids, antioxidant supplements, insulin sensitizers, DHEA, growth hormone, etc.);\n* Use of traditional Chinese medicine within the past 3 months;\n* Known allergy to Coenzyme Q10 or panthenol (water-soluble isomer of CoQ10);\n* PGT (Preimplantation Genetic Testing) population;\n* Acute or chronic renal insufficiency, hemodialysis treatment, history of severe renal impairment;\n* Infectious diseases such as HIV, active hepatitis, history of metabolic acidosis, tuberculosis;\n* Cardiovascular events within 3 months: coronary artery disease\u002Fmyocardial infarction\u002Fclinically significant congestive heart failure; stroke\u002Ftransient ischemic attack; deep vein thrombosis\u002Fpulmonary embolism; uncontrolled hypertension (systolic ≥160 mmHg or diastolic ≥90 mmHg); diagnosed diabetes; coronary intervention or coronary artery bypass graft surgery;\n* Neurological disorders such as dementia (e.g., Alzheimer's\u002FParkinson's) or use of related medications;\n* History of psychological\u002Fpsychiatric disorders and use of antiepileptic, antidepressant, or similar medications;\n* History of cancer, radiation therapy, or chemotherapy;\n* Unwillingness to take supplements provided by this study;\n* Alcoholics, smokers, or individuals with substance dependence;\n* Participants in other clinical trials within the past month;\n* Patients deemed ineligible for enrollment by the investigator.","FEMALE","20 Years","39 Years",{"count":20,"type":21},128,"ESTIMATED","INTERVENTIONAL",[24],"NA","This prospective, randomized, double-blind, controlled study will be conducted at Tangdu Hospital, Air Force Medical University. It plans to enroll 128 patients with poor ovarian response for a 2-year study. The primary objective is to investigate the effects of exogenous coenzyme Q10 supplementation as pre-treatment on ovarian function and assisted reproductive clinical outcomes in patients with poor ovarian response.\n\nStudy Hypothesis: Coenzyme Q10 therapy is expected to effectively enhance ovarian function and improve assisted reproductive outcomes in patients with poor ovarian response, while demonstrating favorable safety profiles.",[27],"Ovarian Response",[29],"Ovarian function","NOT_YET_RECRUITING","2026-07-08",{"date":33,"type":34},"2026-07-13","ACTUAL",{"date":36,"type":21},"2026-07",{"date":38,"type":21},"2027-03",{"name":40,"class":41},"Tang-Du Hospital","OTHER",{"id":43,"slug":4,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":44,"targetDuration":4,"studyType":22,"phases":45,"briefSummary":25,"conditions":46,"keywords":47,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":48,"lastUpdatePostDateStruct":49,"startDateStruct":51,"completionDateStruct":53,"leadSponsor":54,"locationsCount":4},"100612991",{"count":20,"type":21},[24],[27],[29],"2025-12-04",{"date":50,"type":34},"2025-12-05",{"date":52,"type":21},"2025-12",{"date":38,"type":21},{"name":40,"class":41}]