Radiographic Contrast To Differentiate Cavitated From Non-cavitated Tooth Decay
Primary Purpose
Dental Caries
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Sodium iodide
Sponsored by
About this trial
This is an interventional diagnostic trial for Dental Caries
Eligibility Criteria
Inclusion Criteria:
- Must have a minimum of 2 adjacent teeth so that interproximal surfaces of interest are in contact and hidden from direct visual examination.
The occlusal plane plane should be normal so that the interproximal contact regions are normal.
English or Spanish speaker.
Exclusion Criteria:
- Pregnant women. A person who has participated in a similar study involving dental radiography within the last 12 months.
Fillings must not be present in the regions of interest.
Sites / Locations
- Creighton University School of Dentistry
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Contrast
Arm Description
All subjects will be in one group who will have a control radiograph before applying sodium iodide to interproximal surfaces of teeth when another radiograph will be taken to test for the presence of caries cavitation.
Outcomes
Primary Outcome Measures
Number of cavitated versus non-cavitated caries lesions in 116 tooth surfaces.
The PI will perform the clinical application of the sodium iodide and radiograph the subject. A control radiograph will be taken of tooth crowns before the application of the contrast. Immediately after the contrast application another radiograph will be exposed. If caries is present a lucency will be seen in the control The test radiograph will show either contrast on the tooth surface (non-cavitated) or below the surface (caviiatetd). Rubber impressions will be made of the tooth surfaces and scanned with a laser to provide a 3D replica which will be the gold standard for presence or absence of cavitation. At a later date 3 independent dentists will be provided with blinded radiographs in a randomized order to report the presence or absence of cavitated cries lesions.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02359279
Brief Title
Radiographic Contrast To Differentiate Cavitated From Non-cavitated Tooth Decay
Official Title
Radiographic Contrast To Differentiate Cavitated From Non-cavitated Tooth Decay
Study Type
Interventional
2. Study Status
Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
August 2015 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
June 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Creighton University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The proposed test is intended to enable dentists to differentiate between cavitated and non-cavitated tooth decay in the areas where teeth are in contact (interproximal surfaces). In these areas, dentists cannot visually inspect for caries, and currently bitewing X-rays (BWs) only correctly detect the presence of enamel decay 15-25% of the time. This low sensitivity can lead to late treatment resulting in unnecessarily large fillings, crowns, pain, root canals, and possible later loss of teeth.
Detailed Description
Tooth sites will be recorded by both tooth number, type of surface (mesial, distal, occlusal), cavitated, non-cavitated, healthy. Radiographs will similarly be scored. Although contrast agents are classified as drugs this is not a study of drug properties or effect on cells since the properties of the agent are already well known and its safety record well established. This study will be recording the radiopacity of the contrast agent on healthy tooth surfaces, non-cavitated tooth surfaces and cavitated tooth surfaces. The outcome for each surface type will be presence or absence of a radiopacity on a radiograph which will be made at the one and only visit for each study subject. The radiograph contains the data from the intervention (placement of contrast agent) and the outcome will be assessed some weeks later after the completion of the data collection.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dental Caries
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Contrast
Arm Type
Experimental
Arm Description
All subjects will be in one group who will have a control radiograph before applying sodium iodide to interproximal surfaces of teeth when another radiograph will be taken to test for the presence of caries cavitation.
Intervention Type
Device
Intervention Name(s)
Sodium iodide
Intervention Description
Comparison of control radiographs made before application of sodium iodide and test radiograph after application.
Primary Outcome Measure Information:
Title
Number of cavitated versus non-cavitated caries lesions in 116 tooth surfaces.
Description
The PI will perform the clinical application of the sodium iodide and radiograph the subject. A control radiograph will be taken of tooth crowns before the application of the contrast. Immediately after the contrast application another radiograph will be exposed. If caries is present a lucency will be seen in the control The test radiograph will show either contrast on the tooth surface (non-cavitated) or below the surface (caviiatetd). Rubber impressions will be made of the tooth surfaces and scanned with a laser to provide a 3D replica which will be the gold standard for presence or absence of cavitation. At a later date 3 independent dentists will be provided with blinded radiographs in a randomized order to report the presence or absence of cavitated cries lesions.
Time Frame
Immediately after application of sodium iodide
10. Eligibility
Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Must have a minimum of 2 adjacent teeth so that interproximal surfaces of interest are in contact and hidden from direct visual examination.
The occlusal plane plane should be normal so that the interproximal contact regions are normal.
English or Spanish speaker.
Exclusion Criteria:
Pregnant women. A person who has participated in a similar study involving dental radiography within the last 12 months.
Fillings must not be present in the regions of interest.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Douglas Benn, DDS PhD
Organizational Affiliation
Creighton University & Firefly Health Innovations NE inc
Official's Role
Principal Investigator
Facility Information:
Facility Name
Creighton University School of Dentistry
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68178
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34083157
Citation
Benn DK, Cooper RL, Nunn ME, Edwards SE, Rocha-Sanchez SM. A radiographic method for distinguishing noncavitated from cavitated proximal carious lesions: A proof of concept clinical trial. Oral Surg Oral Med Oral Pathol Oral Radiol. 2021 Dec;132(6):715-726. doi: 10.1016/j.oooo.2021.02.014. Epub 2021 Feb 23.
Results Reference
derived
Learn more about this trial
Radiographic Contrast To Differentiate Cavitated From Non-cavitated Tooth Decay
We'll reach out to this number within 24 hrs