Intra-Operative Radiation Therapy (IORT) Using the IntraBeam® System - A Registry Protocol
Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY
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.
Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:
• Female gender
• Age ≥ 45
• cT1-2N0, \<3.5cm invasive breast cancer, estrogen-receptor positive or DCIS of breast, Grade 1-2, mammographically detected, \< 2.5 cm, estrogen-receptor positive
• Suitable for breast conserving surgery
• No contraindication to radiation
• Mammogram within 6 months of planned procedure
• Fitness for lumpectomy under general anesthesia
• Planned to receive IORT
Locations
United States
New York
Montefiore Medical Center - Moses Campus
RECRUITING
The Bronx
Contact Information
Primary
Jana Fox, MD
jfox@montefiore.org
718-920-4140
Time Frame
Start Date: 2018-08-09
Estimated Completion Date: 2032-08
Participants
Target number of participants: 500
Related Therapeutic Areas
Sponsors
Leads: Albert Einstein College of Medicine