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Prospective Open-label Single-arm Single-center Clinical Trial Study on Wuji Baifeng Tablets in the Monotherapy of Ovarian Reserve Dysfunction of Qi and Blood Deficiency Type

Prospective Open-label Single-arm Single-center Clinical Trial Study on Wuji Baifeng Tablets in the Monotherapy of Ovarian Reserve Dysfunction of Qi and Blood Deficiency Type

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000638
Enrollment
Unknown
Registered
2025-04-02
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

diminished ovarian reserve

Interventions

Treatment group:Wuji Baifeng Tablets

Sponsors

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) Female patients between the ages of 18-40 years; (2) Meets the diagnostic criteria of DOR; (3) Those who meet the syndrome of qi and blood deficiency in traditional Chinese medicine; (4) Those who voluntarily participate in this clinical observation and can cooperate with the requirements of treatment and follow-up; (5) The informed consent process complies with the regulations and the informed consent form is signed.

Exclusion criteria

Exclusion criteria: (1) Pregnant women lactating women or women who have planned to conceive in the past six months; (2) Patients with other endocrine diseases (such as endometriosis polycystic ovary syndrome thyroid disease hyperprolactinemia adrenal tumors etc.) and organic lesions of reproductive organs in addition to DOR; (3) Drugs or complementary treatments related to DOR (including: acupuncture traditional Chinese medicine Chinese patent medicine and other complementary alternative medicine therapies) in the past 8 weeks; (4) Those who have used hormone drugs or drugs that affect reproductive endocrine and metabolism in the past 12 weeks; (5) Patients with organic lesions in important organs such as heart lungs liver kidneys etc. or patients with mental disorders and other reasons that cannot cooperate with the test; (6) Those who are allergic to the test drug and its excipients; (7) Those who are undergoing other aspects of treatment or participating in other clinical experimental research; (8) Those who are judged by the investigator to be inappropriate to be selected for this trial.

Design outcomes

Primary

MeasureTime frame
Follicle-Stimulating Hormone;

Secondary

MeasureTime frame
estradiol;luteinizing hormone;anti-Mullerian hormone;Treg;IL-2;growth differentiation factor 9;T helper cell 17;BMP10;IL-4;Traditional Chinese Medicine Syndrome Scoring;GATA-3;transforminggrowthfactor-ß;interferon-?;IL-10;T-bet;antral follicle counting;BMP-15;

Countries

China

Contacts

Public ContactYan Ying

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine

yanying799@163.com18622662859

Outcome results

None listed

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