Actively Recruiting
Intra-Operative Radiation Registry
Led by Albert Einstein College of Medicine · Updated on 2025-09-23
500
Participants Needed
1
Research Sites
729 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This registry trial is designed to track the local control rates and side effects of IORT, which will be implemented for women who are suitable partial breast irradiation (PBI) per the latest American Society of Radiation Oncology (ASTRO) guidelines.
CONDITIONS
Official Title
Intra-Operative Radiation Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female gender
- Age 45 years or older
- cT1-2N0 invasive breast cancer less than 3.5 cm, estrogen-receptor positive or DCIS less than 2.5 cm, Grade 1-2, mammographically detected
- Suitable for breast conserving surgery
- No contraindication to radiation
- Mammogram within 6 months of planned procedure
- Fit for lumpectomy under general anesthesia
- Planned to receive intra-operative radiation therapy (IORT)
You will not qualify if you...
- Known axillary lymph node positive breast cancer
- Multicentric cancer in the same breast not suitable for single lumpectomy with negative margins
- Known BRCA 1 or BRCA 2 gene carriers
- Undergoing neoadjuvant chemotherapy
- Pregnancy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Montefiore Medical Center - Moses Campus
The Bronx, New York, United States, 10467-2490
Actively Recruiting
Research Team
J
Jana Fox, MD
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
0
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