A multicentre parallel control study of breast pain and breast nodules and the true proportion of histology

A multicentre parallel control study of breast pain and breast nodules

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900024100

Enrollment

Unknown

Registered

2019-06-25

Start date

2019-07-01

Completion date

Unknown

Last updated

2019-07-01

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

Conditions

mastalgia and breast nodules

Interventions

psychological intervention:psychological intervention

pharmacological intervention:pharmacological intervention

control group:None

Eligibility

Sex/Gender

Female

Age

30 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Gender: Female (2) Aged 30 years and above; (3) In the past three months, patients have perceptible periodic or non-periodic breast pain and/or ultrasound suggesting nodular changes with exclusion of benign and malignant breast tumors by ultrasound, mammography, and magnetic resonance.

Exclusion criteria

Exclusion criteria: (1) Patients who have previously or currently been diagnosed breast tumors (including breast cancer and benign breast tumors) or breast acute and chronic inflammation; (2) Patients who have breast trauma, coronary heart disease, acute and chronic pulmonary inflammation, tumor, tuberculosis, and psychoneurosis previously; (3) Pregnant or lactating women.

Design outcomes

Primary

Measure	Time frame
questionnaire survey;ultrasonography;palpation;imageological examination;biopsy;	—

Countries

China

Contacts

Public ContactXinyu Zheng

First Affiliated Hospital, China Medical University

xyzheng@cmu.edu.cn+86 024-83282741

Outcome results

None listed

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