Clinical Trials Logo

Clinical Trial Summary

According to the World Health Organization, breast cancer is the most common cancer in women, and is responsible for 686,000 new cases every year. The WHO also posit that nearly 420,000 women perished from the disease in 2002. Surgery remains the best option for patients presenting with operable Stage I, II or III cancers. Breast conservation surgery has been shown to be as efficacious as mastectomy. About 60-70% of these women with operable breast cancer are breast conservation candidates. However, the need to achieve negative tumor margins often requires a second operation (re-excision) in up to 70% of the women having lumpectomy surgery. Currently, tumor margins assessment in the operating room is often assessed grossly by palpation. The ability to evaluate tumor margin using our proposed intraoperative imaging technique may provide the surgeon with an alternative, and hopefully, more sensitive method to assess tumor margins which may decrease re-excision and the morbidity associated with additional surgery, and, perhaps, lower the risk of local regional recurrence.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01796041
Study type Interventional
Source Abramson Cancer Center of the University of Pennsylvania
Contact
Status Completed
Phase Early Phase 1
Start date July 2011
Completion date November 9, 2016

See also
  Status Clinical Trial Phase
Active, not recruiting NCT01644669 - Safety and Efficacy Study of the Xoft® Axxent® eBx® IORT System® N/A
Withdrawn NCT04349111 - An Efficacy Study of the Xoft® Axxent® eBx® IORT System® "Lite" N/A
Active, not recruiting NCT01038258 - Monitoring Response After The First Chemotherapy Cycle After Neoadjuvant Breast Cancer Therapy N/A
Terminated NCT02365714 - CyberKnife Stereotactic Accelerated Partial Breast Irradiation (SAPBI) Phase 1/Phase 2