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A Single Arm Study of Efficacy and Functional Quality of Life in Patients Treated With Transoral Robotic Surgery for Oropharyngeal and Supraglottic Squamous Cell Carcinoma


N/A
18 Years
N/A
Open (Enrolling)
Both
Oropharyngeal Squamous Cell Carcinoma, Supraglottic Squamous Cell Carcinoma

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Trial Information

A Single Arm Study of Efficacy and Functional Quality of Life in Patients Treated With Transoral Robotic Surgery for Oropharyngeal and Supraglottic Squamous Cell Carcinoma


Inclusion Criteria:



- Adult male or female

- Diagnosis of either oropharyngeal or supraglottic squamous cell carcinoma

Exclusion Criteria:

- Metastatic disease

Type of Study:

Interventional

Study Design:

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Progression-free survival

Outcome Description:

Duration of time from date of surgery to date of recurrence or death

Outcome Time Frame:

3 years

Safety Issue:

No

Principal Investigator

Mark J Jameson, MD, PhD

Investigator Role:

Principal Investigator

Investigator Affiliation:

University of Virginia School of Medicine

Authority:

United States: Institutional Review Board

Study ID:

SCCA-TORS-2012

NCT ID:

NCT01819480

Start Date:

March 2013

Completion Date:

Related Keywords:

  • Oropharyngeal Squamous Cell Carcinoma
  • Supraglottic Squamous Cell Carcinoma
  • Surgery
  • Robotic
  • Carcinoma
  • squamous cell of head and neck
  • Carcinoma
  • Carcinoma, Squamous Cell

Name

Location
University of Virginia Health System Charlottesville, Virginia  22903