Actively Recruiting

Age: 55Years +
FEMALE
Healthy Volunteers
NCT06375798

Clinical Study of Breast Conserving Surgery Combined With Intraoperative Radiotherapy for Early Breast Cancer

Led by Hebei Medical University Fourth Hospital · Updated on 2025-09-15

620

Participants Needed

1

Research Sites

313 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

A Single-center, open, prospective study,for analyzing the local recurrence rate, the incidence of incision complications and the aesthetic effect of intraoperative radiotherapy in early breast cancer patients after breast-conserving surgery.

CONDITIONS

Official Title

Clinical Study of Breast Conserving Surgery Combined With Intraoperative Radiotherapy for Early Breast Cancer

Who Can Participate

Age: 55Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 55 years or older
  • Confirmed invasive breast cancer or ductal carcinoma in situ (DCIS) at clinical stage Tis-1N0M0
  • Willing to preserve the breast and undergo breast-conserving surgery
  • Negative surgical margin of at least 2 mm for invasive cancer or at least 3 mm for DCIS
  • Estrogen receptor (ER) 30% or higher, progesterone receptor (PR) 1% or higher, and HER2 negative
  • Voluntary participation with signed informed consent and ability to comply with follow-up
Not Eligible

You will not qualify if you...

  • Diagnosis of bilateral or multifocal breast cancer
  • Previous breast cancer on the same side or prior chest wall radiation
  • Active connective tissue diseases like scleroderma or systemic lupus erythematosus affecting the chest
  • Any other condition deemed unsuitable for study participation by investigators

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Fourth Hospital of Hebei Medical University

Shijiazhuang, Hebei, China

Actively Recruiting

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Research Team

C

cuizhi GENG, archiater

CONTACT

M

meiqi WANG, attending

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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