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Clinical Registry of Long-Term Dental Outcomes in Head and Neck Cancer Patients

Clinical Registry of Long-Term Dental Outcomes in Head and Neck Cancer Patients (ORARAD II)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05325970
Acronym
ORARAD II
Enrollment
202
Registered
2022-04-13
Start date
2014-02-01
Completion date
2026-02-04
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Diseases, Head and Neck Cancer, Osteoradionecrosis

Keywords

dental outcomes, cancer, registry

Brief summary

The current study (ORARAD II) will examine participants of the original cohort for a visit roughly 7 years after the start of RT. The primary outcomes will be the 7-year rate of dental caries, periodontal disease, tooth loss, osteoradionecrosis and salivary flow.

Detailed description

This is a prospective cohort study to document long-term dental and other oral outcomes in patients who receive external beam and modern radiation therapy (RT) modalities with curative intent, as part of clinical care for a head and neck cancer. Five hundred and seventy-two participants were enrolled in the original study, ORARAD, which included a baseline oral examination prior to the start of radiation therapy and follow-up examinations and data collection at six-month intervals up to 2 years after the start of RT. The current study (ORARAD II) will examine participants of the original cohort for a visit roughly 7 years after the start of RT. The primary outcomes will be the 7-year rate of dental caries, periodontal disease, tooth loss, osteoradionecrosis and salivary flow.

Interventions

None listed

Sponsors

Wake Forest University Health Sciences
Lead SponsorOTHER
National Institute of Dental and Craniofacial Research (NIDCR)
CollaboratorNIH
University of Minnesota
CollaboratorOTHER
UConn Health
CollaboratorOTHER
University of Pennsylvania
CollaboratorOTHER
Brigham and Women's Hospital
CollaboratorOTHER
NYU Langone Health
CollaboratorOTHER
University of North Carolina
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Enrolled in the original ORARAD study * Willing to participate and comply with all study procedures

Exclusion criteria

* Anything that would place the participant at increased risk or preclude the participant's full compliance with or completion of the study (e.g., unable to obtain consent or unable to tolerate an oral examination).

Design outcomes

Primary

MeasureTime frameDescription
Dental Caries7 yearsDental caries will be ascertained through the examination parameters outlined by NHANES, and the results of this examination with be used to calculate DMFS scores.
Bleeding on probing is documented (yes/no) (Periodontal Measure 1)7 yearsBleeding on probing is documented (yes/no) and a percentage of "yes" responses will be calculated.
Clinical attachment loss (CAL) (Periodontal Measure 2)7 yearsClinical attachment loss (CAL) measured in mm
Pocket depth (Periodontal Measure 3)7 yearsPocket depth measured in mm
Tooth Loss7 years"Tooth loss" will be defined as a dental extraction that has been performed or recommended. Change in number of teeth throughout the duration of the study will be documented.
Exposed intraoral bone7 yearsExposed intraoral bone is documented clinically by a trained clinical examiner and assessed based on a visual examination of the area, documenting the related tooth numbers or area and the following clinical signs: pain, swelling, induration, sequestrum, thin skin and/or beard loss (i.e. tissue hypoxia), evidence of pathologic fracture, tooth mobility, altered sensation in the affected area. The percentage of patients experiencing exposed bone, their recovery rates, and percent experiencing the signs will be calculated.
Salivary flow7 yearsSalivary flow is measured by the whole stimulated salivary flow rate. Changes in the rate and any association with other outcomes (e.g., caries) will be calculated.

Secondary

MeasureTime frameDescription
Trismus measurements in mm7 yearsChange in mouth opening are documented in mm
7-year use of fluoride7 yearsPatients complete a questionnaire on use of fluoride (other than over the counter toothpaste), type, and frequency. Percent compliance with fluoride use and change in fluoride use will be calculated.
Compliance with brushing/flossing7 yearsPatients complete a questionnaire on frequency of brushing and flossing. Percent compliance with brushing and flossing guidelines (2x per day according to evidence-based professional guidelines) and change in compliance will be calculated.
Changes in RT-specific quality of life measures7 yearsPatients complete a likert scale questionnaire on 10 quality of life measures based on the European Organization for Research and Treatment of Cancer questionnaire. Ten individual question items were scored on a four-point scale indicating level of difficulty with daily tasks (1=not at all; 2=a little; 3=quite a bit; 4=very much).
Change in pain scores7 yearsPatients complete a likert scale questionnaire on pain levels during 8 daily activities rating their pain from no pain (0) to the worst pain imaginable (5) based on the European Organization for Research and Treatment of Cancer questionnaire.
Mortality7 years
Cancer recurrence7 years

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORMichael T. Brennan, DDS, MHS

Wake Forest University Health Sciences

PRINCIPAL_INVESTIGATORRajesh V. Lalla, DDS, PhD

UConn Health

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 30, 2026