Post-Radiation Oral Health in Underserved Head and Neck Cancer Patients
NCT07556367 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120
Last updated 2026-04-29
Summary
This is a pilot study evaluates the feasibility and outcomes of providing fluoride varnish treatment during routine cancer surveillance visits for post-radiation head and neck cancer patients with limited access to dental care.
Conditions
- Head and Neck Cancer
- Head and Neck Carcinoma
- Head and Neck Neoplasms
Interventions
- OTHER
-
Surveys
Participants will complete surveys to collect information about their dental health before and after fluoride varnish treatment. Healthcare and dental providers will complete a survey to assess the feasibility of the fluoride varnish treatment.
- PROCEDURE
-
Saliva Collection
Participants will provide a saliva sample for pH measurement.
- PROCEDURE
-
Intra-oral photographs
Images of participants' teeth will be taken to assess the Decayed, Missing, and Filled Teeth (DMFT) index.
- DEVICE
-
Fluoride Varnish Treatment
Participants will receive 4-5 fluoride varnish treatment every 3 month over the course of a year. Treatment is delivered during cancer surveillance visits. Participant will also receive dental care educational materials.
- OTHER
-
Interview (Participant)
Participants and caregivers will share their experiences accessing dental care, identify barriers to care, and provide their views on integrating preventive dental care into routine medical care. Healthcare and dental providers will share their observations about patient access to dental care and their views on integrating preventive dental care into routine medical care.
Sponsors & Collaborators
-
University of California, San Francisco
lead OTHER
Principal Investigators
-
Mary J Xu, MD · University of California, San Francisco
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-10-01
- Primary Completion
- 2026-10-01
- Completion
- 2026-10-01
- FDA Device
- Yes
Countries
- United States
Study Locations
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