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Treatment of mammary gland hyperplasia by Pre-acupuncture therapy based on Meridian differentiation: a clinical study

Treatment of mammary gland hyperplasia by Pre-acupuncture therapy based on Meridian differentiation: a clinical study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100041666
Enrollment
Unknown
Registered
2021-01-01
Start date
2021-01-31
Completion date
Unknown
Last updated
2021-03-22

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

Conditions

Hyperplasia of mammary glands

Interventions

pre-acupuncture intervention Group:Acupuncture treatment
Oral drug RuPiXiao control group:Take Oral drug RupiXiao

Sponsors

The First Affiliated Hospital of Yunnan University of Chinese Medicine /Yunnan Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Those who meet the diagnostic criteria of mammary gland hyperplasia and in line with TCM syndrome differentiation and classification. 2. Women aged 18 to 55 years whom with Normal menstrual cycle (Definition of Normal menstrual cycle 28±7days). 3. Those who sign the informed consent form, are voluntary subjects, have good compliance, and are able to complete the treatment course. 4. Those who have not received other drug treatment or other relevant intervention measures for breast hyperplasia within 6 months.

Exclusion criteria

Exclusion criteria: 1. Pregnant and lactating women; 2. Those who with a clear family history of breast cancer; 3. Those who with malignant breast tumors; 4. Those who with cardiovascular and cerebrovascular diseases, hepatic and renal insufficiency, hematopoietic diseases and endocrine diseases; 5. Those who with mental disorders and unable to cooperate with the treatment research plan; 6. Those who are participating in other clinical trials. PS:Subjects who meet any of the above exclusion criteria shall be excluded.

Design outcomes

Primary

MeasureTime frame
E2;P;PRL;T;LH;FSH;Breast ultrasound;CA15-3;

Secondary

MeasureTime frame
Breast pain grade;Breast lumps size grading;score of Scope of breast lumps;Breast lumps hardness grade;Body concomitant symptom score;

Countries

China

Contacts

Public ContactRong Zhao

The First Affiliated Hospital of Yunnan University of Chinese Medicine/YunNan Provincial Hospital of Traditional Chinese Medicine

kmzhaorong@qq.com+8613888659309

Outcome results

None listed

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