Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05889091

A Study of the Use of Fat Flap Reconstruction to Reduce Neck Injury After Cancer Treatment

Led by Memorial Sloan Kettering Cancer Center · Updated on 2025-10-16

12

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to find out whether the fat ALT flap procedure is a safe and practical option for reducing neck morbidity in HNSCC patients following cancer treatment of the neck. Neck morbidity after radiation therapy and surgery includes difficulty swallowing, neck or shoulder pain, stiffness, swelling, or changes to the appearance of the treated area. In addition, the researchers will find out whether the study procedure is effective at reducing neck morbidity and improving quality of life after cancer treatment. The researchers will measure quality of life by having participants answer questionnaires.

CONDITIONS

Official Title

A Study of the Use of Fat Flap Reconstruction to Reduce Neck Injury After Cancer Treatment

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 18 years or older
  • Diagnosed with head and neck squamous cell carcinoma (HNSCC), such as oropharyngeal or hypo/laryngeal SCC
  • Primary treatment with radiotherapy, with or without chemotherapy
  • Salvage neck dissection indicated for persistent or recurrent nonmucosal disease in cervical lymph nodes
  • Additional flap coverage needed during salvage neck dissection to improve carotid coverage or replace missing skin
Not Eligible

You will not qualify if you...

  • Patients with primary site mucosal recurrence along with neck disease

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Memorial Sloan Kettering Cancer Center (All Protocol Activities)

New York, New York, United States, 10065

Actively Recruiting

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Research Team

E

Evan Matros, MD

CONTACT

J

Jennifer Cracchiolo, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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