Sentinel Lymph Node Biopsy for Cutaneous Squamous Cell Carcinoma of the Head and Neck

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this study is to research if a type of biopsy known as sentinel lymph node biopsy (SLNB) can help in determining the rate of tumor deposits that are hard to detect and identify in node-negative cutaneous squamous cell carcinoma of the head or neck.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients ≥ 18 years old at the time of informed consent

• Ability to provide written informed consent and HIPAA authorization

• Primary or recurrent invasive cutaneous squamous cell carcinoma of the head or neck, clinically staged T2-T4 based on AJCC staging

• Clinically and radiographically regional node-negative (no evidence of regional lymph node metastasis or distant metastasis)

• Able to undergo general anesthesia for sentinel lymph node biopsy

• Able to undergo CT scan with contrast or MRI with contrast

• Undergo surgical resection (Moh's or micrographic resection or standard excision with sentinel lymph node biopsy) within 8 weeks of imaging

Locations
United States
Indiana
Indiana University Melvin & Bren Simon Cancer Center
RECRUITING
Indianapolis
Contact Information
Primary
Azeezat Yekinni
ayekinn@iu.edu
317-529-6883
Backup
Jessica Yesensky, MD
317- 948-3226
Time Frame
Start Date: 2021-10-25
Estimated Completion Date: 2026-09
Participants
Target number of participants: 94
Treatments
Other: Procedure/Surgery
Mohs micrographic surgery followed by sentinel lymph node biopsy
Sponsors
Leads: Indiana University

This content was sourced from clinicaltrials.gov

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