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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05976295
Other study ID # 20223BBG71012-2
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date August 31, 2023
Est. completion date December 1, 2025

Study information

Verified date September 2023
Source Jiangxi University of Traditional Chinese Medicine
Contact Liang Ruining
Phone 0086-0791-88385243
Email jack169@sina.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Polycystic ovary syndrome (PCOS) is a common reproductive disease associated with endocrine and metabolic disorders. Some studies have shown that Chinese herbal medicine is beneficial for PCOS, but the efficacy of Chinese herbal medicine in the treatment of PCOS is not clear, because the quantity of pre-clinical data was limited and the quality of clinical evidence was variable. Therefore, this randomized double-blind placebo-controlled trial aim to evaluate the efficacy of Chinese herbal medicine (Jianpi Qushi Huatan Decoction) in women with PCOS.


Recruitment information / eligibility

Status Recruiting
Enrollment 68
Est. completion date December 1, 2025
Est. primary completion date September 1, 2025
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: 1. The diagnosis of PCOS is based on the Rotterdam criteria. 2. Meet the syndrome differentiation standard of spleen deficiency and phlegm-dampness in TCM theory. 3. women aged 18-40 years without fertility requirements. 4. A willingness to undergo this treatment plan. Exclusion Criteria: 1. Hyperprolactinemia (2 times serum prolactin levels of more than 25 ng/ml at least one week apart). 2. Diminished ovarian reserve, FSH (follicle-stimulating hormone) level more than 10 IU/L. 3. Abnormal thyroid function, TSH (thyroid stimulating hormone) level less than 0.2 mIU/mL or more than 5.5 mIU/mL. 4. Suspected Cushing's syndrome. 5. Adrenal or ovarian tumors secreting androgen. 6. Poorly controlled type II diabetes. 7. Pregnancy or lactation. 8. Hypertensive patients with poorly controlled blood pressure (a systolic blood pressure more than 160 mmHg or a diastolic blood pressure more than 100 mmHg). 9. Those who had taken hormones or other drugs during the previous 3 months. 10. Acute heart, liver, kidney or blood diseases.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Jianpi Qushi Huatan Decoction
The treatment group will receive the Jianpi Qushi Huatan Decoction (consisting of Radix astragali, Atractylodes Lancea, Dioscorea oppositifolia, Cyperus rotundus, Lindera aggregata, Aconitum gymnandrum and Ligusticum wallichii, among others). Subjects will take the medication from the first day of inclusion, dissolving and consuming one packet twice a day (morning and evening) for a total of three months.
Placebo
The control group will receive a placebo treatment.

Locations

Country Name City State
China The Second Affiliated Hospital of Jiangxi University of Traditional Chinese Medicine Nancang Jiangxi

Sponsors (1)

Lead Sponsor Collaborator
Jiangxi University of Traditional Chinese Medicine

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ovulation rate Ovulation rate in each group during the study period. 3 months
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