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Study on the effect and mechanism of Xiaoangtiaojing Decoction on endometrial receptivity of Qi stagnation and dampness stasis PCOS patients

Study on the effect and mechanism of Xiaoangtiaojing Decoction on endometrial receptivity of Qi stagnation and dampness stasis PCOS patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089407
Enrollment
Unknown
Registered
2024-09-09
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Polycystic ovarian syndrome

Interventions

Control group:On the 5th day of the menstrual cycle, Diane-35 was taken orally once a day for 21 consecutive days. Continuous medication for 3 menstrual cycles.
Treatment group:On the basis of the control group, Xiaoangtiaojing Decoction of traditional Chinese medicine granules was added on the 5th day of menstrual cycle, one dose a day, divided into morning

Sponsors

Henan Province Hospital of TCM
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
21 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. In line with the diagnostic criteria of PCOS Western medicine and the standard of TCM syndrome differentiation; 2. 21 = age = 35 years old and have fertility requirements; 3. Color ultrasound thickness < 7mm during embryo implantation window period; 4. Uterus, ovary and fallopian tube examination are normal, no other diseases affecting conception and pregnancy; 5. Did not receive hormone therapy for 3 months prior to treatment; 6.Those who voluntarily participate in the experiment and sign the informed consent;

Exclusion criteria

Exclusion criteria: 1.There were clinical manifestations of hyperandrogenemia caused by other diseases; 2.There were other causes of abnormal ovulation disease; 3.Patients who have taken drugs such as contraceptives within the last 3 months that may affect the effect and outcome of this study, or who are allergic to the drugs used in this study; 4.Patients with severe primary diseases of cardiovascular and blood system, severe liver and kidney dysfunction and mental illness; 5.Those who failed to follow the doctor 's advice. This study does not comply with, do not cooperate, easy to produce lost to follow-up ; 6.Accompanied by other physiological or pathological conditions that may affect the observation and judgment of the effect indicator; If the samples were receiving drug therapy at the time of selection and met the inclusion criteria after the washout period, they were not considered excluded cases.

Design outcomes

Primary

MeasureTime frame
Endometrial Thickness;Anti-Müllerian Hormone;Insulin -like Growth Factor BindingProtein – 1;Uterine artery pulsatility index;Uterine artery resistance index;Fasting insulin level;Insulin resistance index;miR-155;miR-194;

Secondary

MeasureTime frame
Chinese medicine syndrome scores;Fasting blood glucose;Testosterone;Luteinizing Hormone;Follicle-stimulating hormone;Lnterleukin-6;

Countries

China

Contacts

Public ContactYanyan Zhou

Henan Province Hospital of TCM

zyy19760803@126.com+86 135 2664 9210

Outcome results

None listed

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