Caries,Dental Clinical Trial
Official title:
Diagnostic Ability of Near Infrared Transillumination (NIRT, CariVu™) for Detecting Interproximal Caries as Compared to Conventional Bitewing Radiographs
NCT number | NCT05362461 |
Other study ID # | 19-1142 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | October 31, 2022 |
Est. completion date | January 31, 2023 |
Specific Aims 1. To determine the diagnostic efficacy of CariVu and BWX for detecting interproximal carious lesions in primary dentition BWX and CariVu images will be taken in random order. Number and depth of interproximal carious lesions will be determined by two independent examiners using both CariVu images and BWX. Intra- and inter-rater agreement and disagreement will be determined for all the images and radiographs. 2. To determine acceptability and comfort of CariVu and BWX as perceived by patient, parent and independent observer BWX and CariVu images will be taken in a random order and patient and parent will be given a questionnaire to complete as exit survey. The questionnaire will include few questions to determine perceived acceptability and comfort by parent and patient for either methods (CariVu and BWX). An independent observer (dental assistant) who is masked for the hypothesis of the study will be given a similar questionnaire to evaluate patient behavior using standard behavior assessment scales. 3. To determine difference in chair-side time required for BWX and CariVu image generation Time required to generate both, BWX and CariVu images will be documented by an independent observer (dental assistant) who is masked for the hypothesis of the study and will be compared to determine the overall clinical chair-side time required for generating diagnostic images for efficient and accurate treatment planning
Status | Recruiting |
Enrollment | 50 |
Est. completion date | January 31, 2023 |
Est. primary completion date | December 31, 2022 |
Accepts healthy volunteers | |
Gender | All |
Age group | 5 Years to 9 Years |
Eligibility | Inclusion Criteria: - Pediatric patients from 5-9 years of age - Justification for this age range: Patients younger than 5 years may have open contacts between primary molars. - Patients more than 9 years may have advanced root resorption and primary teeth might be at advanced stages of exfoliation - Patients with American Society of Anesthesiologists classification (ASA)-I or II category (medically healthy) - Parent or legal guardian should consent BWX [per American Academy of Pediatric Dentistry (AAPD) guidelines] and CariVu ™ (Dexis) imaging to be completed during same visit - All selected patients should be in primary or mixed dentition stage with well-established contacts between posterior teeth - Patient with Frankl behavior assessment score of 3 ("positive") or 4 ("definitely-positive") - Patient and parent speaking English or Spanish as their preferred language Justification for language: Language barriers may pose challenges to behavior management in pediatric dental patient and thereby reducing the acceptability of dental treatment (confounding factor). Exclusion Criteria: - Patients with ASA III or IV (medically complex or special health care needs patient) - Patients with open contacts between teeth or missing teeth - Patients who do not need conventional bitewing radiographs per AAPD guidelines - Patient with Frankl behavior assessment score of 1 ("definitely negative") or 2 ("negative") |
Country | Name | City | State |
---|---|---|---|
United States | Children's Hospital Colorado | Aurora | Colorado |
Lead Sponsor | Collaborator |
---|---|
University of Colorado, Denver | Children's Hospital Colorado |
United States,
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* Note: There are 18 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of carious lesions | Number of carious lesions will be determined as a numerical value. | Through study completion, an average of 36 months | |
Primary | Patient and parental perceived acceptability and comfort | Exit survey with 3 questions with binary responses will be provided to parents and patients. | Through study completion, an average of 36 months | |
Primary | Behavior assessment by an independent observer | An independent observer (dental assistant) who is masked for the hypothesis of the study will be given a similar questionnaire to evaluate patient behavior using standard behavior assessment scales. Score will be assessed on Frankl Score Behavior Scale. Frankl Scoring is as follows:
Frankl 1 Definitively Negative Refusal of treatment, forceful crying, fearfulness, or any other overt evidence of extreme negativism Frankl 2 Negative Reluctance to accept treatment, uncooperativeness, some evidence of negative attitude but not pronounced (sullen, withdrawn) Frankl 3 Positive Acceptance of treatment; cautious behavior at times; willingness to comply with the dentist, at times with reservation, but patient follows the dentist's directions cooperatively Frankl 4 Definitively Positive Definitely positive. Good rapport with the dentist; interest in the dental procedures, laugher and enjoyment |
Through study completion, an average of 36 months | |
Primary | Time required for generation of either images (CariVu and BWX) | Both CariVu and BWX images will be taken for routine diagnosis (not an intervention as both images are taken as routine procedures during dental visit). Time to take images will be measured in seconds. | Through study completion, an average of 36 months | |
Primary | Depth of carious lesion | Depth will be measured on a 0-4 point ordinal scale. This scale is as follows:
0- No presence of lesion Caries lesion visible in enamel Caries lesion visible in enamel with single point contact to the dentino-enamel junction Caries lesion visible in enamel extensive contact to the dentino-enamel junction Caries lesion visible in enamel and dentin |
Through study completion, average of 36 months |
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