Skip to content

Clinical Efficacy and Mechanism of Tiaojing Yuluan Decoction in the Treatment of Polycystic Ovary Syndrome

Clinical Efficacy and Mechanism of Tiaojing Yuluan Decoction in the Treatment of Polycystic Ovary Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001523
Enrollment
Unknown
Registered
2026-06-20
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

PCOS

Interventions

Group A (Lifestyle Interventions):Receive basic lifestyle interventions (in accordance with the 2023 International Evidence-Based Guidelines for PCOS), under the guidance of trained researchers or nut
Group B (lifestyle interventions + Tiaojing Yulu Decoction oral solution):Undergo basic lifestyle interventions: take 1 dose per day, divided into 2 servings, starting from the first day of menstruati
Group C (Lifestyle intervention + Metformin Hydrochloride Tablets):Undergo basic lifestyle interventions. Initial dose: 0.5 g per dose, once daily (taken with dinner)
for 1 week.
Group D (lifestyle intervention + Tiaojing Yulu Decoction oral solution + Metformin Hydrochloride tablets):Participants received basic lifestyle interventions. They took medications in the same manner

Sponsors

Liuzhou Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Ages 20–40 years; meeting the diagnostic criteria of both Western and traditional Chinese medicine; have not used hormonal medications, metformin, ovulation-stimulating drugs, or traditional Chinese medicine treatments in the past 3 months; willing to sign the informed consent form.

Exclusion criteria

Exclusion criteria: Hyperandrogenemia due to other causes; thyroid dysfunction; severe cardiac, hepatic, or renal insufficiency (ALT/AST >2.5 times the upper limit of normal, Cr >115 µmol/L); diabetes mellitus (fasting blood glucose =7.0 mmol/L or use of hypoglycemic medications); mental illness or cognitive impairment; participation in other clinical trials at the same time.

Design outcomes

Primary

MeasureTime frame
rates of normalization of menstrual cycles;follicular fluid non-targeted metabolomics;

Secondary

MeasureTime frame
rates of ovulation rates;luteinizing hormone;Insulin resistance index;ALT;rates ofpregnancy rates; testosterone;follicle-stimulating hormone; estradiol;traditional Chinese medicine syndrome scores;blood lipid levels; body mass index; waist circumference;AST; Cr; BUN;blood tests; urine tests; electrocardiogram;adverse events;targeted metabolomics;correlation networks; ROC prediction models;

Countries

China

Contacts

Public ContactJING JING LI

Liuzhou Maternal and Child Health Hospital

7407lijingjing@163.com18977286362

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Aug 10, 2026