Clinical trial · Interventional
Post-Radiation Oral Health in Underserved Head and Neck Cancer Patients
NCT07556367CI-TRIAL-00113094active not recruitingN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Head and Neck Cancer | Malignant Head and Neck Neoplasm | ALIAS | 0.90 |
| Head and Neck Carcinoma | Head and Neck Carcinoma | ONTOLOGY_EXACT | 0.98 |
| Head and Neck Neoplasms | Head and Neck Neoplasm | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (5)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Fluoride Varnish Treatment | Device | — | UNRESOLVED |
| Interview (Participant) | Other | — | UNRESOLVED |
| Intra-oral photographs | Procedure | — | UNRESOLVED |
| Saliva Collection | Procedure | — | UNRESOLVED |
| Surveys | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Fluoride Varnish Treatment (Participant)
- description
- Participants will received Medicom Duraflor Ultra White 5% Sodium Fluoride varnish treatments during their routine cancer surveillance visits every 3-6 month for about 1 year. During these visits, participants will complete short surveys, provide saliva samples, and have photos taken of their teeth before and after the treatment. Health and dental care providers will also be asked to complete a survey about fluoride treatment delivered.
- interventionNames
- Other: Surveys
- Procedure: Saliva Collection
- Procedure: Intra-oral photographs
- Device: Fluoride Varnish Treatment
- type
- OTHER
- label
- Interview
- description
- The research team will interviews with participants, caregivers, and healthcare and dental providers.
- interventionNames
- Other: Interview (Participant)
Primary outcomes (2)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. \>18 years old who are uninsured or underinsured (MediCal, Healthy SF) or have full coverage. 2. Patients who have received immunotherapy or enhanced chemotherapy regimens. 3. Patients or health and dental care providers who are able to provide their own informed written consent. Exclusion Criteria: 1. \>18 years old. 2. Patients, caregivers, health and dental care providers who are able to provide their own informed written consent.
References
Publications (0)
Data not yet available
No reference posted for this study.