Using ultrasound to diagnose periodontal diseases early
High Frequency Intraoral Ultrasound Probe for Early Diagnosis of Periodontal Diseases
This study is testing a new ultrasound tool to see if it can help dentists diagnose gum diseases more accurately and comfortably than the usual methods.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 65 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Tours Academic / other |
| Locations | 1 site (Tours) |
| Trial ID | NCT05809427 on ClinicalTrials.gov |
What this trial studies
This clinical investigation aims to evaluate the accuracy of a high-frequency intraoral ultrasound probe in measuring periodontal pocket depth compared to traditional periodontal probing, which is considered the gold standard. The study is conducted in two phases: the first phase involves collecting ultrasonic images to train an Artificial Intelligence module for better measurement accuracy, while the second phase assesses the performance of the ultrasound device for quicker and more comfortable periodontal assessments. The goal is to improve the diagnostic process for periodontal diseases.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older with at least 10 teeth and evidence of periodontal disease.
Not a fit: Patients who have undergone recent surgical procedures in the area to be scanned or those with specific legal protections may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to earlier and more accurate diagnosis of periodontal diseases, improving patient outcomes.
How similar studies have performed: While the use of ultrasound in dental diagnostics is emerging, this specific approach has not been widely tested, making it a novel investigation.
Eligibility criteria
Show full inclusion / exclusion criteria
Patient Inclusion Criteria : Age ≥ 18 years Affiliated to a social security scheme Free, informed and signed consent Ability for participant to comply with the requirements of the study Exclusion Criteria (patient): Surgical procedure performed in the area to be scanned Osteosynthesis material Under legal protection Pregnant women, breastfeeding Teeth Inclusion Criteria Minimum of 10 teeth One tooth from each sextant Presence of at least 1/3 of pathological sites (\>4mm and/or deep sites \>6mm)
Where this trial is running
Tours
- University hospital of Tours — Tours, France (Recruiting)
Study contacts
- Study coordinator: Fréderic DENIS, PR
- Email: frederic.denis@univ-tours.fr
- Phone: 0033247471400
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.