Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
300

Summary

Conditions
  • Oral Cavity Squamous Cell Carcinoma
  • Oropharynx Squamous Cell Carcinoma
  • Squamous Cell Carcinoma of the Head and Neck
  • Squamous Cell Carcinoma of the Oropharynx
Type
Observational
Design
Observational Model: Case-ControlTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

A noninvasive point of care salivary rinse test performed as 1) a one-time test for control subjects, 2) at pretreatment and post treatment 3,6, 12, and 18 month time points in oral cavity/oropharynx cancer patients

A noninvasive point of care salivary rinse test performed as 1) a one-time test for control subjects, 2) at pretreatment and post treatment 3,6, 12, and 18 month time points in oral cavity/oropharynx cancer patients

Tracking Information

NCT #
NCT03148665
Collaborators
  • Vigilant Biosciences, Inc.
  • Greater Baltimore Medical Center
  • San Diego Veterans Healthcare System
  • NYU Langone Health
  • Johns Hopkins University
Investigators
Study Chair: Joseph Califano, MD University of California, San Diego