Clinical Trial

Study Comparing Limited and Extensive Neck Surgery in Oral Cancer Patients With Neck Spread

Study acronym: ExtentN1
Recruiting
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Summary
Oral cavity squamous cell carcinoma (OCSCC) frequently metastasizes to cervical lymph nodes, and the extent of neck dissection remains an area of ongoing debate in patients with clinically node-positive (cN1) disease. While modified neck dissection (MND, levels I-V) is widely practiced, selective neck dissection (SND, levels I-IV) may provide equivalent oncologic outcomes with reduced surgical morbidity. However, high-quality randomized evidence comparing these approaches is lacking. The ExteNT N1 Trial is a prospective, randomized, open-label, parallel-group clinical trial designed to compare selective neck dissection (levels I-IV) with modified neck dissection (levels I-V, preserving the spinal accessory nerve, internal jugular vein, and sternocleidomastoid muscle) in patients with resectable cN1 oral cavity squamous cell carcinoma. Eligible participants will be randomized in a 1:1 ratio to either treatment arm. The primary endpoint is 3-year regional recurrence-free survival (RRFS), along with postoperative quality of life measured using the Neck Dissection Impairment Index (NDII). Secondary endpoints include overall survival, disease-free survival, level-wise nodal involvement, nodal yield, shoulder function (Constant-Murley Score, SPADI, and Arm Abduction Score), postoperative complications including chyle leak, and other surgical morbidities. This trial aims to generate level I evidence regarding the optimal extent of neck dissection for cN1 OCSCC, balancing oncologic safety with preservation of postoperative function and quality of life.
Protocol Amendment History 1 change
critical Recruitment opened 2026-08-05
Trial Details
NCT Number NCT07717307
Lead Sponsor Kolhapur Cancer Centre - Cancer Centers of America
Conditions Oral Cavity Squamous Cell Carcinoma
Enrollment 80 participants
Start Date 2026-08-01
Primary Completion 2031-04-22 (estimated)
Study Completion 2031-04-23 (estimated)
Updated on ClinicalTrials.gov 2026-08-04