Breast Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with invasive breast cancer confirmed by a tissue sample (biopsy).
- People whose cancer is at a certain stage (classified as T0–3, T4b and N0–3a) and who need chemotherapy before surgery.
- People who do not have cancer that has spread to other parts of the body.
- People who are planned to receive radiation therapy after surgery and are considered suitable for a type of breast reconstruction called a DIEP flap at the time of their mastectomy.
Who may not be able to join:
- People who are already taking part in another clinical trial that could affect the results of this study.
- People who received chemotherapy before surgery but do not have an indication for radiation therapy.
- People whose cancer continued to grow or spread during chemotherapy before surgery.
- People who are pregnant or currently breastfeeding.
- People who have a previous history of diabetes.
- People who have a previous history of heavy smoking.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Jiong Wu, Fudan University
Phone: 862164175590
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Patient satisfaction with breasts questionnaire Patient satisfaction of breast
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.