Caries Detection With Two Different Caries Detecting Devices
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Tufts University
- Study ID
- NCT06152081
- Status
- Recruiting
Conditions
- Caries,Dental
Eligibility Criteria
- Sex
- ALL
- Age
- 21 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- LumiCare rinse — DEVICEThe teeth being assessed will be cleaned of any debris ,plaque and calculus. The areas being assessed will be air dried. A dry field will be maintained using cotton rolls and a saliva ejector. Lumicare rinse will be applied onto the test areas for 30 seconds and the excess removed using a saliva ejector. The sites will then be rinsed with plain water for 10 seconds and excess will be removed using high volume suction. A blue curing light will then be held 1-2 inches from the test surfaces while the examiner assesses the surfaces for the presence or absence of fluorescent illumination.
- QLF Inspektor Pro Imaging — DEVICEThe teeth being assessed will be cleaned of any debris ,plaque and calculus. The areas being assessed will be air dried. A dry field will be maintained using cotton rolls and a saliva ejector. The QLF device will be positioned over the tooth surface to be tested and an image will be taken. The images will be stored automatically and assessed by the examiners for the presence of green fluorescence using the QA2 program (Version 1.25, Inspektor Research systems BV, Amsterdam, The Netherlands) . The trend in green fluorescence will also be calculated using this software algorithm.
Study Details
The primary aim of this study will be to compare the effectiveness of the novel LumiCare™ rinse and with QLF in determining caries progression. The secondary aim is to compare the progression of carious lesions between patients who reported use of e-cigarettes/vapes and those who did not.
Key Dates
- Start date
- Apr 1, 2025
- Status verified
- Aug 2025
- Primary completion
- Apr 30, 2026
- Completion
- Oct 31, 2027
Study Design
- Enrollment
- 60 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- DIAGNOSTIC
Arms
- Experimental: All ParticipantsAll participants enrolled in the study will have the two caries detecting devices used during each research visit.
Primary Outcome Measure
Comparison of two caries-detecting devices [ Time Frame: 12 months ]
Central Contacts
- Karina Irusa, BDS,MS6176362408
- Ann-Marie Billig6176363931
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Tufts University School of Dental Medicine | Boston | Massachusetts | 02111 | - |
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