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Study on hyperplasia of mammary glands treated with external therapy programmes and evaluation

Study on hyperplasia of mammary glands treated with external therapy programmes and evaluation

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002920
Enrollment
Unknown
Registered
2012-09-22
Start date
2010-05-01
Completion date
Unknown
Last updated
2017-04-18

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

Treatment group:ointment bilateral breast
Control group:Placebo

Sponsors

The Third affiliated Hospital of Beijing University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. with breast hyperplasia disease diagnosis standard; 2. at the age of 18 ~ 50 years old women ( including 18 and 50 years old), basic rules of the menstrual cycle and period. Menstrual cycle for 28 days - 7 days; 3. in group VAS>3 patients, pain of moderate pain; 4. previous cyclic premenstrual breast pain symptoms, course lasts for more than 3 months; 5. did not receive the treatment of hyperplasia of mammary glands, within six months not using hormonal preparations; 6. breast skin intact, no damage, no skin disease; 7. informed consent, voluntary subjects and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. with breast hyperplasia disease diagnostic criteria, but does not have the cyclical breast pain; 2. associated with malignant breast tumor, inflammatory disorders and other endocrine diseases; 3. the menstrual cycle or period serious irregular; 4. with cardiovascular, hepatic, renal, hematopoietic system of severe primary disease, or psychiatric patients; 5. during pregnancy, lactation, menopause and preparation of pregnant women; 6. allergic constitution or known to the medicine component or allergy; 7. taking parting in other clinical drug trials.

Design outcomes

Primary

MeasureTime frame
Breast pain;Breast tumor size;Routine blood test;Urine routine test;

Secondary

MeasureTime frame
Curative effect of disease;TCM Comprehensive Treatment;Estradiol;Progesterone;Prolactin;quality of life;

Countries

China

Contacts

Public ContactPei Xiaohua
pxh_127@163.com+86 010 52075253

Outcome results

None listed

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