If the subject is sentinel node positive and meets study requirements, the subject is
randomized to receive either (1) completion lymphadenectomy (2) observation with nodal
ultrasound. Subjects are then followed for 10 years.
For more information about a clinical trial, clinical trial eligibility, or informed consent, contact our research nurses by phone or email:
- Cancer Help Line: (800) 639-6918
- Email: email@example.com
Please Note: Any eligibility criteria noted are subject to change. Our research nurses can provide you with the most current eligibility and exclusion criteria. Any study involvement to be undertaken must ultimately be determined on an individual basis.