Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 1:13 AM
Ignite Modification Date: 2025-12-25 @ 1:13 AM
NCT ID: NCT05459493
Eligibility Criteria: Inclusion Criteria: 1. The age range of patient is 18-40 years old. 2. Women with DOR, and wish to improve ovarian function or menopausal syndrome. The diagnostic criteria for DOR is as follows: If two of the following three tests of ovarian reserve function are met, DOR can be diagnosed: bilateral AFC\<6; AMH \< 1.1 ng/ml; 10 mIU/ml \<bFSH\<25 mIU/ml. 3. Sign the informed consent form. Exclusion Criteria: 1. Patient is known to be allergic or unsuitable for the Chinese herbal compound. 2. Women who are pregnant and lactating. 3. Patients had been menopause for more than 1 year. 4. Abnormal uterine bleeding, except ovulation disorders. 5. Women is taking hormone drugs and has stopped taking them within 3 months; 6. Women with endometriosis, myadenosis, submucosal fibroids or the size of non-submucosal fibroids is more than 4 cm. 7. The nature of pelvic mass is unknown. 8. Women with polycystic ovary syndrome, hyperprolactinemia, hyperandrogenemia, diabetes, thyroid and adrenal dysfunction and other endocrine diseases affecting ovulation. 9. Patients with serious primary diseases such as cardiovascular, liver, kidney, lung, biliary, hematopoietic system (Hb\<90g/L) and malignant tumor, and psychiatric patients. 10. Patients are participating in other clinical trials or have participated in other clinical trials within the last month. 11. Unsuitable for the study evaluated by the investigator.
Healthy Volunteers: False
Sex: FEMALE
Minimum Age: 18 Years
Maximum Age: 40 Years
Study: NCT05459493
Study Brief:
Protocol Section: NCT05459493