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NCT01473784Recruiting

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

A Pilot Study Assessing Transoral Robotic Surgery (TORS) for Oral and Laryngopharyngeal Benign and Malignant Lesions Using the Da Vinci Robotic Surgical System

Source: ClinicalTrials.gov · Last updated 10 Feb 2026

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Study type
Interventional
Enrollment
600 (estimated)
First submitted
7 Nov 2011
Start date
3 Dec 2007
Primary completion date
31 Dec 2026
Lead sponsor
Ohio State University Comprehensive Cancer Center
NCT number
NCT01473784

What you commit to

  • Study type: Interventional
  • Planned participants: 600
  • From 3 Dec 2007 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous head and neck surgery that would preclude transoral/robotic procedures. This is at the investigator's discretion. This is not an exclusion criterion for the non-surgical arm.
  • Inability to adequately visualize anatomy to perform the diagnostic or therapeutic surgical approach transorally

Other illness

  • Unexplained fever and/or untreated, active infection
  • The presence of medical conditions contraindicating general anesthesia or transoral surgical approaches

Other

  • Patient pregnancy
  • Inability to grant informed consent
  • INTRAOPERATIVE EXCLUSION CRITERIA:

Who the study is looking for

  • Patient must present with indications for diagnostic or therapeutic approaches for benign and/or malignant diseases of the oral cavity or laryngopharynx (including the neoplastic lesions of the tongue, tongue base, retromolar trigone, tonsils, palate, posterior and lateral pharynx, glottic, supraglottic and subglottic larynx)
  • Patients must have adequate transoral exposure of the oral cavity and laryngopharynx for TORS instrumentation
  • Written informed consent and/or Consent waiver by institutional review board (IRB)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ohio State University Medical Center
Coordinator of this site? Confirm its status
ColumbusUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.