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Clinical study of ZiYu Prescription in the treatment of polycystic ovary syndrome

Clinical study of ZiYu Prescription in the treatment of polycystic ovary syndrome

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006557
Enrollment
Unknown
Registered
2022-09-02
Start date
2022-09-01
Completion date
Unknown
Last updated
2023-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

polycystic ovary syndrome

Interventions

1:ZiYu Prescription+dydrogesterone
2:placebo+dydrogesterone

Sponsors

Shuguang Hospital affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) It meets the diagnostic criteria of Western medicine for polycystic ovary syndrome and the diagnostic criteria of traditional Chinese medicine for renal deficiency; (2) Between the ages of 18 and 40. (3) Have not taken any drugs that affect menstruation (such as contraceptives, hormones or other drugs that affect insulin, blood glucose, sex hormones and lipid metabolism) within 3 months and have not used relevant treatment methods, and have no record of induced abortion; (4) Gynecological examination and auxiliary examination: there are no organic lesions of internal and external genitalia, and there are no other primary diseases; (5) Sign the patient's informed consent form.

Exclusion criteria

Exclusion criteria: (1) The presence of congenital deficiencies in the patient's reproductive system cannot meet the needs of this study. (2) The patient has a congenital inherited mental illness. (3) The patient's liver, heart, kidney, hematopoietic system and other human organ functions are failed. (4) The patient has a special physique and has a history of serious allergies to the drug. (5) Patients who cannot be performed according to this study protocol. (6) Patients with other diseases need to undergo other aspects of treatment, and patients who may have an impact on this study. (7) Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Days of menstrual cycle;

Secondary

MeasureTime frame
FINS;E2;FPG;AMH;FSH;TC;LDL;T;LH;TG;

Countries

China

Contacts

Public ContactBingYi Yang
jszxyby@126.com13816938605

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026