Randomized Phase II/III Trial of Sentinel Lymph Node Biopsy Versus Elective Neck Dissection for Early-Stage Oral Cavity Cancer
- Sponsor:
- NRG
- Sponsor Study ID:
- HN006
- CTO #:
- 103517
- NCT Number:
- NCT04333537
- Phase:
- II/III
- Protocol Type:
- Treatment
- Age Group:
- Adults
- Disease Sites:
- Lip, Oral Cavity and Pharynx
- Study Objectives:
- This phase II/III trial studies how well sentinel lymph node biopsy works and compares sentinel lymph node biopsy surgery to standard neck dissection as part of the treatment for early-stage oral cavity cancer. Sentinel lymph node biopsy surgery is a procedure that removes a smaller number of lymph nodes from your neck because it uses an imaging agent to see which lymph nodes are most likely to have cancer. Standard neck dissection, such as elective neck dissection, removes many of the lymph nodes in your neck. Using sentinel lymph node biopsy surgery may work better in treating patients with early-stage oral cavity cancer compared to standard elective neck dissection.
- eConsent:
- Not available
- Study Documents:
-
Open Study Documents
(MUSC NetID required for document access)
For more information about this trial please contact the study team:
-
Medical University of South Carolina
- Principal Investigator, Graboyes, Evan, at graboyes@musc.edu , or please call +1 414-331-4721.
- Study Coordinator, Avinger, Madison, at avingerm@musc.edu .
Trial opened at the following institutions:
Medical University of South Carolina