Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT01473784

Transoral Robotic Surgery in Treating Patients With Benign or Malignant Tumors of the Head and Neck

Led by Ohio State University Comprehensive Cancer Center · Updated on 2026-02-10

600

Participants Needed

1

Research Sites

995 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This pilot clinical trial studies transoral robotic surgery (TORS) in treating patients with benign or malignant tumors of the head and neck. TORS is a less invasive type of surgery for head and neck cancer and may have fewer side effects and improve recovery

CONDITIONS

Official Title

Transoral Robotic Surgery in Treating Patients With Benign or Malignant Tumors of the Head and Neck

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient must need diagnostic or therapeutic procedures for benign or malignant diseases in the oral cavity or laryngopharynx, including lesions of the tongue, tonsils, palate, pharynx, and larynx
  • Patients must have adequate transoral exposure for robotic surgery instruments
  • Written informed consent or institutional review board approved consent waiver must be provided
Not Eligible

You will not qualify if you...

  • Unexplained fever or untreated active infection
  • Pregnancy
  • Prior head and neck surgery that prevents transoral robotic procedures, as determined by the investigator
  • Medical conditions that prevent general anesthesia or transoral surgery
  • Unable to give informed consent
  • During surgery, inability to adequately see anatomy to perform transoral surgical approach

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

Ohio State University Medical Center

Columbus, Ohio, United States, 43210

Actively Recruiting

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Research Team

O

Ohio State University Comprehensive Cancer Center

CONTACT

C

Chelsea Marra

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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